PlainRecordsBrand recall history
Cordis US recalls
Every FDA recall record we found for Cordis US, newest first. Updated Oct. 11, 2026.
7
7 recalls since 2022. The most recent was on April 9, 2025.
- Last 12 months
- 0
- Most recent
- 2025-04
- Most serious (FDA Class I)
- 2
- Last 30 days
- 0
Recalls by year
2022–20262223242526
Class I (FDA, most serious)Other recalls
All recalls
7- April 9, 2025Cordis… and 1 more product Class IIproduct mix-up; Vascular stent labeled as one size but contains a different size.
- March 19, 2025Vista Brite Tip… Class IICatheter manufactured at the incorrect length.
- Jan. 17, 2024Mynxgrip 5F… and 1 more product Class IICordis became aware that the label for the carton box containing 10 units is incorrect for some boxes of two lots of MynxGrip. The carton box from…
- Nov. 15, 2023Cordis ANGIOGRAPHIC CATHETERIZATION SETS… Class INon-sterile product labeled as sterile was distributed.
- May 17, 2023ANGIOGUARD RX / XP Emboli Capture Guidewire System… and 13 more products Class IThere is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of…
- Dec. 21, 2022Cordis Angiographic Catheter Extensions… Class IIThere is a potential for separation at the male connector.
- July 20, 2022PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System… Class IIPotential for stent dislodgement and associated failures related to two specific sizes of the device.
No recalls match.
How we match: a recall is listed here when the agency names Cordis US as the company that filed it. Sources: FDA enforcement reports and FDA-posted company announcements, CPSC recall notices and NHTSA recall campaigns.