PlainRecordsBrand recall history
Amendia recalls
Every FDA recall record we found for Amendia, newest first. Updated Oct. 11, 2026.
8
8 recalls since 2016. The most recent was on Jan. 17, 2018.
- Last 12 months
- 0
- Most recent
- 2018-01
- Most serious (FDA Class I)
- 0
- Last 30 days
- 0
Recalls by year
2016–20261617181920212223242526
Class I (FDA, most serious)Other recalls
All recalls
8- Jan. 17, 2018Mac Pin Non-Cannulated Screw… Class IIIncorrect labeling for the lot of MAC Pins. Although the pins are laser as 460 mm in length, the pins are 60 mm in length.
- Jan. 10, 2018Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws are self-drilling variable screws that are… Class IIIncorrect direct marking and color identification for the affected lot of Ceres Self-Drilling Variable Screws. Although the laser mark and color…
- May 3, 201701.4mm x 457mm (18in) K-Wire… Class IIMislabeled guide wires - It was discovered that some Guide Wires labeled as stainless steel were actually manufactured from nitinol.
- Jan. 18, 2017Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device… Class IIAbsent tantalum market pin.
- Dec. 28, 2016Optimus Fixed Awl Class IIComplaints that the tip of the awl broke after impaction during surgery.
- Dec. 28, 2016Black Widow Plate 19mm Plate… and 1 more product Class IIThere is a problem with the mating feature between the plate and screw which could cause the plate opening not to interfere enough with the plate and…
- Dec. 28, 2016K-Wire 1.4mm x 12in Non-Threaded… and 2 more products Class IIThe rods are packaged in packages with unacceptable seals. In some cases, the integrity of the seal is compromised by channels or voids.
- Dec. 28, 2016Zeus-P Lumbar Interbody Device Class IILabeling error where three boxes in inventory had conflicting patient and primary labels. Evaluation indicated that the primary label and patient…
No recalls match.
How we match: a recall is listed here when the agency names Amendia as the company that filed it. Sources: FDA enforcement reports and FDA-posted company announcements, CPSC recall notices and NHTSA recall campaigns.