Stryker Sustainability Solutions: Catheter, Recording, Electrode, Reprocessed
Stryker Sustainability Solutions is recalling reprocessed Medtronic Marinr Steerable electrophysiology catheters (Product Number 72402) distributed nationwide in the US and in Canada and Israel due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the medical device. This is a Class II recall affecting hospitals and medical facilities that received these products.
- Recalling firm
- Stryker Sustainability Solutions
- Product
- Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Reason
- Incomplete seals on sterile product
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-10
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide and the countries of Israel and Canada.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2959e91f-8700-464f-9a6d-86126e6d52cf