Device may fracture during use at the laser welded joint on the pointer tube. If this happens, loose parts may fall out of the product while the device is inside the patient.
Filed by: Stryker Leibinger GmbH & Co. KG · Also listed under Stryker Leibinger
More recalls
600 in all years
Nov. 4, 2026Nalu TD2 Therapy Disc with firmware…Class IITherapy Disc (TD) that powers and sends stimulation signals to an Implantable Pulse Generator (IPG), part of a neurostimulation system, has a… Recall began Sept. 30, 2026
Nov. 4, 2026Orthoscan VERSA Accessory Cart…Class IIThe accessory cart weldment does not conform to weld dimensional specifications which may result in separation of the monitor arm mounting structure… Recall began Sept. 3, 2026
Nov. 4, 2026OmniaSecure Model 3930M…Class IIAffected leads require additional engineering evaluation due to complaints regarding difficulty in achieving fixation during implantation. Potential… Recall began Sept. 17, 2026
Oct. 28, 2026PNE Lead Implant Kit REF: 1701Class IIRetroactively Reported: 10mL luer lock syringes included in kit may leak , break or experience other issues that may pose a risk to users. Recall began July 15, 2024
Oct. 28, 2026Medtronic NDI Passive Spheres REF: 8801071… and 3 more productsClass IISterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to… Recall began Aug. 31, 2026
Oct. 28, 2026B Braun SAFSITE Injection Site…Class IIPotential for leakage and backflow at the Safsite valve. Recall began Sept. 14, 2026
Oct. 28, 2026Philips Lumify Diagnostic Ultrasound SystemClass IUltrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which… Recall began Sept. 24, 2026
Oct. 21, 2026Williams Cystoscopic Injection Needles…Class IIThe female Luer lock adapter component in the affected device lots may not have been correctly seated due to misalignment and inadequate torquing… Recall began Sept. 16, 2026
Oct. 21, 2026LeadCare II Blood Lead Test Kit…Class IIIIn kit sub-lot 2530M-01 the date of expiration printed on the outer labeling may indicate the wrong expiration date of July 22, 2026 while the… Recall began Sept. 4, 2026
Oct. 21, 2026DxU 840m Iris… and 1 more productClass IIThe rinse-line check valve has a shorter service lifespan than originally expected and requires annual replacement to prevent lamina fluid leakage… Recall began Aug. 12, 2026
Oct. 21, 2026iFuse TORQ Implant System Model/Catalog Number: 10055T(10x55mm)…Class IIThe pelvic fixation screws failed to meet acceptance criteria for tube packaging seal integrity testing; therefore, sterility assurance cannot be… Recall began Aug. 21, 2026
Oct. 21, 2026Power F2 Powered Fastening System…Class IIFirmware issue may result in intermittent loss or degradation of powered functionality when paired with compatible stretcher. The issue may lead to… Recall began April 28, 2026
Oct. 21, 2026NaviFlex LW Pusher…Class IIDevice was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with… Recall began Sept. 10, 2026
Oct. 21, 2026JenaValve Trilogy Delivery Catheter… and 2 more productsClass IIDelivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device. Recall began July 31, 2026
Oct. 14, 2026Intellijoint Navigation System: Workstation G2 Configured…Class IIA navigation system used to aid in selection and positioning of orthopedic implant system components has a workstation that may contain a 15-inch… Recall began Aug. 28, 2026
Oct. 14, 2026SEDIPLAST…Class IIDuring use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause… Recall began Aug. 25, 2026
Oct. 14, 2026DAVINCI TRUCUSTOM BUNDLE… and 14 more productsClass IIProduct may be potentially contaminated with a lubricant used during the manufacturing process. Recall began Aug. 10, 2026
Oct. 14, 2026Battle Bandage…Class IICompression bandage may be degraded, which may cause unwanted foreign material to be introduced inside the wound, which may lead to wound exploration… Recall began Sept. 2, 2026
Oct. 14, 2026Spectral CT and Spectral CT 7500 RT…Class IISoftware issues may affect the safety and performance of Spectral CT system(s). The issues may result in image artifacts, wrong slice thickness, or… Recall began Aug. 21, 2026
Oct. 7, 2026Salata Salad Kitchen Jalapeno Avocado Dressing…Class IThis recall was initiated due to potential Salmonella contamination in diced jalapeno received from the supplier Recall began Aug. 6, 2026
Oct. 7, 2026CHARLOTTE CLAW Screw…Class IIScrews, intended for use with polyaxial compression plating system intended for foot osteotomies, was manufactured with missing threads on the… Recall began Aug. 18, 2026
Oct. 7, 2026Intrapulmonary Percussive Ventilation… and 6 more productsClass IILabeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV… Recall began Aug. 18, 2026
Oct. 7, 2026Computed Tomography X-ray System… and 11 more productsClass IIPositron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS… Recall began Aug. 11, 2026
Oct. 7, 2026McKesson CONSULT hCG Urine Cassette… and 3 more productsClass IIhCG rapid tests may detect low levels of hCG below the stated assay sensitivity, which may result in false positive result. Recall began Aug. 20, 2026
Oct. 7, 2026HeartSine samaritan PAD (Public Access Defibrillator)…Class IIIProducts were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check. Recall began July 27, 2026
Oct. 7, 2026VentStar Resus Neo…Class IPotential cracks in the hose, which could lead to leakage or the hose falling off. Recall began Sept. 3, 2026
Oct. 7, 2026NovaSeq 6000Dx including DRAGEN Server…Class IIRetrospectively reported correction for an instrument intended for targeted sequencing of DNA libraries from human genomic DNA used with in vitro… Recall began Sept. 17, 2024
Oct. 7, 2026Brand Name: Ferndale Laboratories…Class IIDue to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits. Recall began Jan. 15, 2026
Sept. 30, 2026Presource Convenience Kits: 1) KIT… and 1 more productClass IIThe kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator. Use of a potentially contaminated… Recall began Aug. 10, 2026
Sept. 30, 2026Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234Class IIDue to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing… Recall began Aug. 7, 2026
Sept. 23, 2026Reign Medical Clench Staple System (Compression)…Class IIBone fixation staple requires a new 510(k); the performance characteristics of this device have not been adequately established. Recall began July 15, 2026
Sept. 23, 2026Happiest Baby… and 1 more productClass IIExtra small (ES) and Extra-large (XL) infant sleep sacks have not been reviewed for safety and effectiveness by the FDA. Recall began Aug. 7, 2026
Sept. 23, 2026GM Helix Implant…Class IIThere is a discrepancy between the product identification on the packaging and the dimensions of the implant contained inside. Recall began Aug. 12, 2026
Sept. 23, 2026Plum administration sets and 7 more productsClass IIIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored… Recall began May 12, 2026
Sept. 16, 2026Alfalfa…Class IPotential E. coli and Salmonella contamination
Sept. 16, 2026HeartSine SAM 350P 350P US Device…Class IIDue to a damaged (over stretched) membrane tail that causes an intermittent fault. Recall began July 27, 2026
Sept. 9, 2026Velys Enabling Tech Robotic-Assist Station REF: 451611001Class IISoftware issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning. Recall began July 23, 2026
Sept. 9, 2026Baxter Novum IQ Syringe Pump… and 1 more productClass IIA software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be…
Sept. 9, 2026HEALON EndoCoat PRO…Class IISurgical instructions sent for viscoelastic products used during ophthalmic viscosurgical cataract procedures including in part: If resistance is… Recall began July 31, 2026
Sept. 9, 2026STA Staclot Protein S…Class IIA positive drift in QC values within the reagent's stated 4-hour onboard stability period was identified Recall began July 29, 2026
Sept. 2, 2026Medline medical convenience kits… and 3 more productsClass IISpecific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to… Recall began July 8, 2026
Aug. 26, 2026Dairyland Produce…Class IJalapenos may be contaminated with Salmonella.
Aug. 26, 2026Halyard LAVH PACK…Class IIThe kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a… Recall began July 10, 2026
Aug. 26, 2026Arrow-LOK Implant…Class IIImplant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection. Recall began June 23, 2026
Aug. 26, 2026BD Needle Kit for Powered Driver 15mm x 15Ga…Class IAfter placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically…
Aug. 19, 2026ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000Class IIA strong pull on the high-pressure transfer hose of cryosurgical unit may lead to pneumatic short circuit between he gas inlet and the connector… Recall began June 26, 2026
Aug. 19, 2026OBP Medical…Class IIThere is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions… Recall began July 13, 2026
Aug. 19, 2026GM Helix Implant…Class IIThere may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the… Recall began July 13, 2026
Aug. 19, 2026navify Digital Pathology (on-prem) v2.5…Class IIDue to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window Recall began April 20, 2026
Aug. 12, 2026REF # D23352… and 1 more productClass IIAnalyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications." Recall began June 26, 2026
Aug. 12, 2026Anti-Torque…Class IIPedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have… Recall began May 22, 2026
Aug. 12, 2026Brand Name: OXOS Medical…Class IIDue to a defective circuit board that overheats Recall began June 11, 2026
Aug. 5, 2026M5 Corpus Power Wheelchair REF,120032Class IIThis recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive… Recall began June 19, 2025
July 29, 2026Fusia…Class IUndeclared Allergen (Fish) Recall began June 25, 2026
July 29, 2026Flexible Hystero-Fiberscope Kits REF: 11264BBU1…Class IIFlexible hysteroscopes indicated for use during diagnostic and operative hysteroscopic procedures may contain an expired single use endoscopic seal… Recall began May 21, 2026
July 29, 2026SafeOp Patient Interface…Class IIIntraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG)… Recall began May 13, 2026
July 29, 2026MiniMed Go App…Class IIFor MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the… Recall began June 16, 2026
July 29, 2026SnapshotGLO Wound Imaging Device…Class IIThe software controlling the wound imaging device's battery charging circuit was not designed to recognize and recover a battery that has fully…
July 29, 2026Boston Scientific TheraSphere 360 Y-90 Management Platform…Class IISoftware anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more… Recall began June 19, 2026
July 29, 20263mensio Workstation (Vascular Fenestrated) softwareClass IIUser measurement value reported by diagnostic bioimaging software intended to measure/visualize cardiovascular structures may be larger (0.8% to… Recall began May 7, 2026
July 29, 2026SeaSpine Polyaxial Head REF Number: 41-3010Class IIDue to manufacturing error, polyaxial head may popoff from the screw intraoperatively following insertion. Recall began May 28, 2026
July 29, 2026Power F2 Powered Fastening System…Class IIProduct may experience accelerated roller wear and potential deformation due to interference between the roller assembly and rail. In the worst-case… Recall began June 19, 2026
July 22, 2026Orthofix MINIRAIL… and 3 more productsClass IIUnilateral external fixation devices may be incorrectly labeled. Minirail M101 was labeled as M103, Minirail M103 was labeled as M101, and Minirail… Recall began June 10, 2026
July 22, 2026da Vinci SP Instrument Arm Drape…Class IIRobotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the… Recall began May 12, 2025
July 15, 2026High Valley Orchard Chocolate Covered Raisins…Class IUndeclared Peanut. High Valley Orchard Chocolate Covered Raisins contains unintended undeclared peanut due to mis-packaging.
July 15, 2026GSP Neonatal GALT Kit…Class IIReduction in the on-board stability of the GSP GALT assay. This may increase the likelihood of run-QC failures and consequently delay the reporting… Recall began May 18, 2026
July 15, 20265008X Blood Tubing Set…Class IIPotential for Online Port Errors due to connection issues when connecting the SafeLine of the 5008X CAREset to the substitution fluid port of the… Recall began May 11, 2026
July 15, 2026KL Owen Custom Orthodontic Solution…Class IIA product error defect may cause incorrect bracket placement. Recall began June 8, 2026
July 15, 2026Intracept Access Instruments…Class IIIntraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility… Recall began April 22, 2026
July 8, 2026Radius VSM ECG pre-connected Set… and 1 more productClass IITwo devices recalled: 1) Electrocardiogram (ECG) electrode assembly ECG feature may incorrectly detect extreme bradycardia, tachycardia and trigger… Recall began Feb. 20, 2026
July 8, 2026OTP5000 THORA/PARA TRAY… and 13 more productsClass IIDue to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled… Recall began May 21, 2026
July 8, 2026IntelliCuff…Class IIDue to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to… Recall began May 22, 2026
July 8, 2026Depuy Synthes… and 1 more productClass IIThe external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. Recall began May 19, 2026
July 8, 2026Breathing circuit set…Class IVentilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test… Recall began May 29, 2026
July 1, 2026INZONE DETACHMENT SYSTEM…Class IIEmbolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint… Recall began April 6, 2026
July 1, 2026Da Vinci ASSY…Class IIOperative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake… Recall began April 22, 2026
June 24, 2026SaltClass IIIPlain salt was labeled as iodized and iodized salt was labeled as plain. Recall began May 14, 2026
June 24, 2026Great Value Hawaiian Roll 4pk…Class IIFirm observed oily and sticky substance on direct food contact surface packaging of finished product. Recall began May 15, 2026
June 24, 2026Nutrisystem…Class IIUndeclared Allergen (Soy) Recall began May 13, 2026
June 24, 2026iLet Bionic Pancreas…Class IIThe reason for the recall is: it was found in version 3.3.6 of the iLet ACE Pump firmware and all previous releases that a screen unlock failure… Recall began Sept. 23, 2025
June 24, 2026Mito Red Light…Class IIThe near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames. Recall began Feb. 12, 2025
June 24, 2026Ritmed Neurological Sponges… and 1 more productClass IINeurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during… Recall began May 8, 2026
June 24, 2026Impella CP Set with SmartAssist…Class IExposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of… Recall began May 18, 2026
June 24, 2026PARACENTESIS KIT… and 34 more productsClass ILidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have… Recall began April 21, 2026
June 17, 2026Taro Cakes…Class IUndeclared Egg Allergen Recall began Jan. 30, 2026
June 17, 2026MOSAIQ Oncology Information SystemClass IISoftware may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
June 17, 2026Bicarby Dialysate…Class IIThere is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the… Recall began May 7, 2026
June 17, 2026Medartis APTUS…Class IIThe cannulation of the CCS screw is not centered. Recall began April 24, 2026
June 17, 2026Bicarby" Dialysate…Class IIGiven the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for… Recall began May 12, 2026
June 17, 2026Plum Solo Precision IV Pump… and 2 more productsClass IIUnder certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming… Recall began April 29, 2026
June 10, 20261) Cheese Sauce Mix… and 3 more productsClass IProduct contains dry milk powder ingredient recalled by the supplier due to potential Salmonella contamination Recall began May 6, 2026
June 10, 2026My Wife's Slaw… and 1 more productClass IIProduct was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety… Recall began May 5, 2026
June 10, 2026Betaine Anhydrous…Class IIPossible carbon steel foreign material (1-2mm) Recall began Dec. 15, 2025
June 10, 2026Digital Angiography System Trinias:UD150G-40 / D150GC-40…Class IIElectromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off. Recall began April 20, 2026
June 10, 2026PhaseOne Antimicrobial Solution…Class IIThe recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material… Recall began April 27, 2026
June 10, 2026Brand Name: B… and 7 more productsClass IIB. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL Liquid Adhesive, that they have issued a voluntary… Recall began Jan. 29, 2026
June 10, 2026Ivenix Infusion System (IIS)…Class IFresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components… Recall began May 6, 2026
June 10, 2026LVP software of the Ivenix Infusion System (IIS)…Class IPotential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that… Recall began May 6, 2026
June 3, 2026Automated Impella Controller (AIC)…Class IA retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware… Recall began April 20, 2026
May 27, 2026Pork King Good Onion & Sour Cream Seasoning…Class ISeasoning was made with recalled California Dairies milk powder due to Salmonella contamination. Recall began April 23, 2026
May 27, 2026Vitamin B-Complex…Class IIForeign object: black particulate matter
May 27, 2026Atomoxetine Capsules HCL…Class IILabeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.
May 27, 2026Oncology Kit w/60" (152 cm) Appx 2.2 ml…Class IIOncology sets/closed system transfer devices with extension sets may leak resulting in therapy delayed if noticed and corrected during setup, but if… Recall began March 24, 2026
May 27, 2026Swan-Ganz Catheter… and 2 more productsClass IICatheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to… Recall began April 8, 2026
May 20, 2026Diowave Laser System…Class IISoftware update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms… Recall began Jan. 9, 2026
May 13, 2026Fain s Blackberry Honey Spread… and 9 more productsClass IICreamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic. Recall began April 3, 2026
May 13, 2026LIFEPAK 15…Class IISome defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure… Recall began April 13, 2026
May 13, 2026Prodisc C SK U.S… and 1 more productClass IIProduct labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm… Recall began March 20, 2026
May 13, 2026Halyard CARDIAC CATH PACK kit… and 9 more productsClass IPotential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between… Recall began March 13, 2026
May 6, 2026Brand Name: Leksell Vantage Arc System REF: 1053958Class IILocking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures. Recall began March 19, 2026
May 6, 2026iLet Bionic Pancreas…Class IIinsulin pump software versions 1.4.2, and 1.4.3 issue with Dexcom Continuous Glucose Monitoring (CGM) G7 sensor may result in delayed CGM reading… Recall began March 12, 2026
May 6, 2026Depuy Synthes… and 8 more productsClass IIThe external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. Recall began April 3, 2026
May 6, 2026Immy…Class IINeutralization Buffer may contain contaminants Recall began March 26, 2026
April 29, 2026Flamingo Funnel Small… and 2 more productsClass IICertain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape. Recall began March 16, 2026
April 29, 2026Oxoid Agglutinating Sera…Class IIAffected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the… Recall began March 25, 2026
April 22, 2026Gentuity HF-OCT Imaging System Model G10-01…Class IIThe potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx… Recall began March 23, 2026
April 22, 2026iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision SoftwareClass IIit was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI)… Recall began Aug. 13, 2025
April 15, 2026BRAHMS KRYPTOR compact REACT…Class IICustomers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require… Recall began March 12, 2026
April 15, 2026Multi-parameter Command Module…Class IIMulti-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad… Recall began Feb. 27, 2026
April 15, 2026See Luer Cap Set…Class IIMolded Products, Inc. is voluntarily conducting a medical device recall of the MPC-130 See Luer Cap Set based on a confirmed complaint of the… Recall began Feb. 17, 2026
April 15, 2026Tornier HRS Max parts: 1…Class IIAffected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are… Recall began March 5, 2026
April 8, 2026Divided Sunset Multi Collagen Peptides…Class IIThe product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species… Recall began Feb. 27, 2026
April 8, 2026SIGNA Premier systemsClass IIWhole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with… Recall began Feb. 27, 2026
April 8, 2026MiniMed 670G Insulin Pump (MMT-1760… and 13 more productsClass IIAll Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and… Recall began Feb. 13, 2026
April 8, 2026Airway Exam Kit… and 6 more productsClass IIKits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the… Recall began Feb. 16, 2026
April 8, 20262.4 VOLT TAP LOCKING SCREW TAP TO 90MM… and 1 more productClass IIA full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps… Recall began Feb. 25, 2026
April 8, 2026Brand Name: da Vinci S… and 1 more productClass IIDue to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments Recall began Dec. 9, 2025
April 8, 2026Brand Name: da Vinci S… and 3 more productsClass IIDue to increased complaints for broken/frayed grip cables for reusable instruments. Recall began Dec. 9, 2025
April 8, 2026BD Kiestra" ReadA…Class IIIn certain situations, following a system reboot, one or more modules may have become unreachable via the remote connectivity interface. When this… Recall began Feb. 6, 2026
April 8, 2026RefleXion X1 Radiotherapy System Model RXM1000…Class IIDue to a radiotherapy medical system software defect, when performing angular roll corrections followed by a repeat localization, the roll… Recall began Feb. 9, 2026
April 1, 202614" Margarita Thin Crust Pizza…Class IIpotential foreign object (metal pieces) in ingredient (Tomatoes) Recall began Jan. 14, 2026
April 1, 2026Basil Pesto & Mozzarella Pizza… and 1 more productClass IIMetal fragments in bread. The firm discovered metal fragments in various bread products. They determined the cause to be roasted tomatoes provided by… Recall began Jan. 19, 2026
April 1, 2026SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g)…Class IIUndeclared Allergens: Soy & Wheat. The firm was notified by a customer that the product is labeled as Savannah Bee Company Honey BBQ Sauce "Mustard"… Recall began Feb. 27, 2026
April 1, 2026Embrace Drill Tower… and 1 more productClass IIThe surgical technique for the Embrace Shoulder Instruments - Drill Tower has mixed-up article numbers in the overview of the instruments. However… Recall began Feb. 11, 2026
April 1, 2026MiniMed" 780G…Class IIThree software defects (Pump Error 53, BG check, and Critical Pump Error (Open Book Image)) that occurred as a result of software updates (versions… Recall began Jan. 30, 2026
April 1, 2026Handy Solutions Neck & Shoulders Heating Pad…Class IIf heating pad is folded while in use, the power density increases in the folded area causing excessive temperatures, which can also be caused by… Recall began Feb. 18, 2026
April 1, 2026CentrosFLO Hemodialysis Catheters… and 4 more productsClass I16F dual-valved splittable sheath introducer due to a design defect, may not split as intended, which may result in hemorrhage, foreign bodies… Recall began Feb. 13, 2026
March 25, 2026Battery Charging Station…Class IIIThe Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used… Recall began Feb. 6, 2026
March 25, 2026Brand Name: Welch Allyn…Class IIDisplay screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in… Recall began Feb. 18, 2026
March 18, 2026C2O Coconut Water with Pulp (17.5 oz) 15 Pack…Class IIIThe outer cardboard box for the canned coconut water has the incorrect Nutrition Facts Panel and Ingredient List, which does not include added sugar…
March 18, 2026DxC 700 AU… and 1 more productClass IIA delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open… Recall began Jan. 30, 2026
March 18, 2026Raz-AT (Attendant Tilt) Mobile Shower Commode Chair…Class IIDue to a modification by a vendor and may be reinstalled without properly engaging the outside rear seat brackets that are used to keep the seat in… Recall began Jan. 5, 2026
March 18, 202610mL Non-Sterile BD Luer-Lok Tip Syringe Only…Class IIDuring the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. Recall began Jan. 27, 2026
March 11, 2026Gelsoft Plus…Class IIGelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life.… Recall began Dec. 18, 2025
March 11, 2026Esaote Endocavity ultrasonic probe…Class IIA potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the… Recall began March 14, 2025
March 11, 2026Brand Name: B… and 2 more productsClass IIThe potential for the needle tip to be dull/blunt, difficult to advance, and/or break. Recall began Feb. 2, 2026
Feb. 25, 2026Da Vinci 5 ASSY…Class IIAn error event following the release of a software version for the surgical system that can result in loss of user interface content on an external… Recall began Nov. 17, 2025
Feb. 25, 2026MOLLI 2 System System includes: MM1000 (Pack of 10)…Class IIDue to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during… Recall began Jan. 21, 2026
Feb. 18, 2026CREAMY PEANUT BUTTER… and 2 more productsClass IIForeign material. During production, the firm found pieces of blue plastic in a filter. Recall began April 30, 2025
Feb. 18, 2026Barco MNA with the HexaVue IP Integration System…Class IIThis is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter)… Recall began May 23, 2025
Feb. 18, 2026da Vinci 5 Surgeon Console Viewer Display…Class IIRobotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field… Recall began Dec. 30, 2025
Feb. 18, 2026Brilliance iCT… and 3 more productsClass IIAs part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these… Recall began Jan. 7, 2026
Feb. 11, 2026JUICE from the Raw… and 6 more productsClass IUnder-processed product may contain pathogenic bacteria that could harm to humans. Recall began July 24, 2025
Feb. 11, 2026Volk Single Use Vitrectomy Lenses 1… and 12 more productsClass IIThere may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has… Recall began Dec. 16, 2025
Feb. 11, 2026EMPOWR 3D Knee Tibial Insert 5R 14MM… and 1 more productClass II942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices… Recall began Jan. 5, 2026
Feb. 11, 2026Brand Name: Da Vinci Product Name: da Vinci X…Class IIDue to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was… Recall began Nov. 7, 2025
Feb. 11, 2026COULTER DxH Diluent…Class IIDue to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers. Recall began Nov. 10, 2025
Feb. 4, 2026Qunol…Class IIMold contamination detected for raw material lots that were produced in July and used in finished goods. Recall began Dec. 16, 2025
Feb. 4, 2026BEAR Implant…Class IIIncorrect expiration date on label that extends beyond the product's documented/approved shelf life. With an incorrect expiration date, the UDI will… Recall began Dec. 31, 2025
Feb. 4, 2026Evolution Upgrade 1.5T… and 12 more productsClass IIThe potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication… Recall began Dec. 3, 2025
Feb. 4, 2026Conductivity Standard Solution Catalog/Model Numbers: 10001…Class IIdue to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect… Recall began Dec. 12, 2025
Jan. 28, 2026SQ40S Blood Transfusion FilterClass IIDue to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be… Recall began Nov. 3, 2025
Jan. 28, 2026The LDL-Cholesterol assay is comprised of two distinct phases…Class IIBeckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL… Recall began Dec. 8, 2025
Jan. 28, 2026Tego Connector: REF: 011-D1000…Class IINeedle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a… Recall began Dec. 19, 2025
Jan. 21, 2026TESTO-100 CIII (testosterone 100 mg)…Class IILack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets. Recall began Oct. 3, 2025
Jan. 21, 2026Pulsator Arterial Blood Sampling Kit… and 1 more productClass IIAffected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may… Recall began Dec. 19, 2025
Jan. 21, 2026CentriMag Blood Pump…Class IIAcute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the… Recall began Oct. 10, 2025
Jan. 21, 2026da Vinci SP…Class IIAccess Port System tray may develop cracks potentially resulting in a sterility breach. Recall began Dec. 15, 2025
Jan. 21, 2026Brand Name: Catalyst+ Product Name: Catalyst…Class IIDue to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain… Recall began Oct. 9, 2025
Jan. 21, 2026Medicrea… and 1 more productClass IIDue to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant. Recall began Oct. 29, 2025
Jan. 21, 2026VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 and 1 more productClass IIThere is a potential for formation of ice occurring in the venting system of the superconducting magnet of the MRI systems. if a quench occurs in… Recall began Dec. 19, 2025
Jan. 14, 2026Codman Microsensor Basic Kit… and 1 more productClass IIPotential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits. Recall began Dec. 12, 2025
Jan. 14, 2026BD Pyxis ES Enterprise Server Catalog Numbers 1115-00…Class IIDue a software issue that may result in equipment not receiving timely updates of patient, medication, or related information from enterprise systems. Recall began Dec. 3, 2025
Jan. 14, 2026Philips Tempus Pro Patient Monitor…Class IIPatient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for… Recall began Nov. 26, 2025
Jan. 7, 2026BVI Leos Laser and Endoscopy System…Class IIManufacturing deviation in which the ferrites specified for the USB cable assembly linking the Nurse Monitor touchscreen to the System Controller… Recall began Dec. 5, 2025
Dec. 31, 2025da Vinci 5…Class IISurgical system Error 23062 due to connector1) Partially damaged "Potential problem with ergonomics: Disable - Retry " or 2) Failed "Disable… Recall began Aug. 21, 2024
Dec. 31, 2025BD Pyxis MedStation ES…Class IIAutomated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to… Recall began Nov. 20, 2025
Dec. 31, 2025Draeger Vapor 2000… and 1 more productClass IA certain component of affected devices was not delivered within specification and contained impurities. Recall began Nov. 24, 2025
Dec. 24, 2025Alinity ci-series System Control Module (SCM)…Class IIAbbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction. The reason for the… Recall began Nov. 13, 2025
Dec. 24, 2025InPen App…Class IIWhen app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't… Recall began Nov. 13, 2025
Dec. 24, 2025BIOSURE HA SCREW…Class IIRemoval of affected lot of screws due to labeling error. Recall began Nov. 24, 2025
Dec. 24, 20251ml of DTT in liquid phase… and 1 more productClass IITreatment reagent functionality in respiratory specimens liquification cannot be guaranteed. Recall began Oct. 29, 2025
Dec. 24, 2025Intelerad InteleShare software…Class IISoftware intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are… Recall began Nov. 18, 2025
Dec. 24, 2025Orthofix NorthStar OCT Navigation Surgical Technique Guide…Class IIThe NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards… Recall began Nov. 17, 2025
Dec. 24, 2025Ivenix Infusion System (IIS)…Class ISoftware version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death. Recall began Nov. 14, 2025
Dec. 17, 2025Hemodialysis System…Class IIScrew may loosen or fallout of Hemodialysis system Recall began Oct. 27, 2025
Dec. 17, 2025DEXLOCK Achilles Repair Implant Kits…Class IIThere have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit… Recall began Nov. 11, 2025
Dec. 17, 2025Endo Model Knee Fusion Nail SK…Class IIThe device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral… Recall began Nov. 10, 2025
Dec. 10, 2025Reagent Kits/ containing flow cells…Class IIAn instrument intended for sequencing DNA libraries with in vitro diagnostic assays is used with reagent kits including flow cells that have flow… Recall began Oct. 28, 2025
Dec. 10, 2025Lumify Diagnostic Ultrasound System models : 795005…Class IIUltrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining. Recall began Oct. 31, 2025
Dec. 10, 2025Hemochron Activated Clotting Time Low-Range Test Cuvette…Class IITest cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of… Recall began Nov. 5, 2025
Dec. 10, 2025Phantom Fibula Nail…Class IIFibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so… Recall began Oct. 13, 2025
Dec. 10, 2025Ivenix Infusion System (IIS)…Class IIDownstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set. Recall began Nov. 3, 2025
Dec. 10, 2025InSure ONE Fecal Immunochemical Test…Class IIInSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results. Recall began Sept. 17, 2025
Dec. 10, 2025IVENIX INFUSION SYSTEM…Class IIncorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury. Recall began Nov. 3, 2025
Dec. 3, 2025Cold Form Wrap: Back…Class IIThe IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may… Recall began Sept. 25, 2025
Dec. 3, 2025Philips Azurion 7M20 systems with FlexArm ceiling-mounted system…Class IIThe motorized longitudinal movement of the FlexArm stand may be inconsistent (not smooth) and eventually may become unavailable. This issue is due to… Recall began Oct. 2, 2025
Dec. 3, 2025CareLink Clinic…Class IISoftware error causing incorrect data to be displayed on the 24-hour Sensor Glucose Overview Graph, any potential therapy decisions were made based… Recall began Oct. 21, 2025
Dec. 3, 2025Emdogain…Class IIThe possibility for this product that is intended for demonstration purposes only to be placed in patients. Recall began Oct. 17, 2025
Dec. 3, 2025FoundationOne CDx (F1CDx)… and 1 more productClass IIReports were sent to customers without the companion diagnostic (CDx) Claims Page. Claims pages were distributed via amended reports within 7 days of… Recall began Nov. 8, 2022
Nov. 26, 2025Brand Name: ACUSON… and 1 more productClass IIAffected catheters were reprocessed beyond validated cycles. This may compromise device sterility or mechanical integrity of the device and can lead… Recall began Oct. 8, 2025
Nov. 26, 2025Meridian Bioscience… and 1 more productClass IIThe cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume. Recall began Oct. 7, 2025
Nov. 26, 2025PhD Hemostasis Valve…Class IIHemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in… Recall began Aug. 4, 2025
Nov. 26, 2025BD Luer Tip Caps…Class IIBD has confirmed through internal testing that certain device trays failed routine biocompatibility testing. Recall began Oct. 14, 2025
Nov. 19, 2025Loaded Veggie Grain Bowl…Class IIPotential contamination with Listeria monocytogenes Recall began Oct. 7, 2025
Nov. 19, 2025Multichem ID-B… and 1 more productClass IIPotential of negative recovery of the HBsAg analyte across two (2) lots of Multichem ID-B Positive Control when tested on the Alinity i platform. Recall began Oct. 17, 2025
Nov. 19, 2025BD Kiestra" Isolate Suspension Cuvette Array…Class IIThe 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a…
Nov. 19, 2025CEREPAK Detachable Coil System…Class IDetachable coils system may fail to detach, which could result in hemorrhagic and ischemic stroke, procedural delays, or the need for additional… Recall began Oct. 2, 2025
Nov. 12, 2025SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent…Class IIBeckman Coulter has identified that there is an increased probability Synchron Systems Direct LDL Cholesterol (LDLD REF 969706) reagent lot M404166… Recall began Sept. 17, 2025
Nov. 5, 2025Thermo scientific MAS Omni CARDIO…Class IIThe firm received complaints from customers reporting vial-to-vial variability when using the control with high sensitivity Troponin I assays. This… Recall began Oct. 1, 2025
Nov. 5, 2025Model: Incisive CT… and 2 more productsClass IIIssue 1: The potential for unintentional continued gantry/couch movement when a specific button series is used requiring use of manual stop. Issue 2.… Recall began Sept. 25, 2025
Nov. 5, 2025SAFE-T-FILL Micro Capillary Blood Collection…Class IIAll RAM SAFE-T-FILL Micro Capillary Blood Collection tubes manufactured between July 31, 2023 to February 28, 2025 cause false positive results when… Recall began May 5, 2025
Nov. 5, 2025ChemoLock Bag Spike… and 37 more productsClass IIPort weld of drug transfer device may separate or break during use and potentially result in a leak. Recall began Sept. 8, 2025
Nov. 5, 2025Alcon PRECISION1 One-Day Contact Lenses…Class IIPotential for a weak seal in some units resulting in compromise in sterility. Recall began Sept. 30, 2025
Nov. 5, 2025SuRgical Planner (SRP)… and 6 more productsClass IIA software anomaly, under specific conditions when large rotational alignment values are applied in 2D Image Fusion, may lead to misalignment of any… Recall began Sept. 16, 2025
Oct. 29, 2025READY MEALS Pesto Bowtie Pasta Salad… and 9 more productsClass IListeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes. Recall began Sept. 26, 2025
Oct. 29, 2025Arctic Shores… and 4 more productsClass IIProduct manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original… Recall began Sept. 23, 2025
Oct. 29, 2025Frozen Organic Spinach…Class IIOrganic Spinach has the potential to be contaminated with Listeria monocytogenes.
Oct. 29, 2025Basil Pesto Bowtie Pasta Salad… and 1 more productClass IStore-made deli items contain a pasta ingredient that was recalled due to potential Listeria monocytogenes Recall began Sept. 26, 2025
Oct. 29, 2025Floria Dried Apricots…Class IProduct contains undeclared sulfites. Recall began April 29, 2025
Oct. 29, 2025Jumbo Meat Ball Sub…Class IIMozzarella Cheese ingredient potential to be contaminated with metal shavings.
Oct. 29, 2025Zenition 50…Class IIOver time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier… Recall began Sept. 29, 2025
Oct. 29, 2025Fuse ULTRA Foot Plating System Instructions for Use…Class IIInstructions for use for a foot plating system is being updated to remove the second option of requirements for sterilization which was 3 minutes… Recall began Sept. 17, 2025
Oct. 29, 2025LOW PROF LCKNG SCREW… and 1 more productClass IIAlthough the etched length on the screw is correct, the length marked on the external packaging is incorrect. Specifically, 42mm screws were packaged… Recall began Sept. 26, 2025
Oct. 29, 2025iNSitu Bipolar Hip System…Class IIDownstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile… Recall began Sept. 11, 2025
Oct. 29, 2025IV Administration sets…Class IIV Gravity burette administration set burette component is missing an internal shutoff valve intended to stop fluid flow, which if used may result in…
Oct. 22, 2025Dole Apple Juice (primary package)…Class IIA manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability. Recall began Sept. 11, 2025
Oct. 22, 20251. SILVER HORSE…Class IIContains elevated levels of lead Recall began Sept. 18, 2025
Oct. 22, 2025Cardiac Workstation 5000… and 1 more productClass IIFailure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a… Recall began Sept. 12, 2025
Oct. 22, 2025Airvo 2…Class IIWhen unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound… Recall began Sept. 18, 2025
Oct. 22, 2025BioPro Femoral Head (Metal 22… and 5 more productsClass IIPotential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk… Recall began Sept. 9, 2025
Oct. 22, 2025XERF EFFECTOR 60…Class IIManufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients. Recall began Sept. 4, 2025
Oct. 22, 2025FERNO POWER X2 POWERED AMBULANCE COT…Class IIThe fastening post hardware could loosen allowing the fastening post to detach from the cot Recall began Sept. 11, 2025
Oct. 22, 2025Flow Re-Direction Endoluminal Devices: FRED 27…Class IIFlow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be… Recall began Sept. 5, 2025
Oct. 22, 2025Zenith Alpha 2 Thoracic Endovascular Graft…Class IAffected devices may contain PTFE coating scrapings. Scrapings could be released during device deployment, potentially causing intravascular… Recall began Sept. 18, 2025
Oct. 15, 2025Toto S'Mores Ooey Gooey Cookie…Class IIProduct label contains conflicting statements about inclusion and being free of Soy ingredient. Recall began Aug. 20, 2025
Oct. 15, 2025Kirkland Signature brand Ahi Tuna Wasabi Poke…Class IListeria monocytogenes. Recall was initiated after being notified by green onion supplier of a Listeria monocytogenes positive test result in the…
Oct. 15, 2025CorNeat EverPatch… and 1 more productClass IIReviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch. Recall began Aug. 18, 2025
Oct. 8, 2025Shrimp Cocktail Bowl… and 1 more productClass IIProduct manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Oct. 8, 2025Lipton Green Tea Citrus…Class IIUndeclared sugar in finished product-primary package does not reflect the product inside bottle.
Oct. 8, 2025Venclose digiRF Generators…Class IISoftware version 3.35 of the Venclose digiRF Generator incorporates a catheter verification feature specifically designed to detect internal wiring… Recall began Aug. 21, 2025
Oct. 8, 2025JUNCTIONAL EMERGENCY TREATMENT TOOL (JETT)…Class IIDevice used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the… Recall began July 1, 2025