Stryker Sustainability Solutions: Catheter, Recording, Electrode, Reprocessed
Recall Summary Stryker Sustainability Solutions is recalling reprocessed BW Webster Duo-Decapolar electrophysiology catheters (Product Number D728260RT) because some units have incomplete seals on their sterile packaging. The affected catheters were distributed nationwide across the US, as well as in Canada and Israel. This is a Class II recall, meaning the defective packaging could potentially allow contamination of the medical device.
- Recalling firm
- Stryker Sustainability Solutions
- Product
- BW Webster Duo-Decapolar, Product Number D728260RT; 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/0028227b-8946-47cb-bf04-1c75a2871e45