Stryker Sustainability Solutions: Catheter, Recording, Electrode, Reprocessed
Recall Summary Stryker Sustainability Solutions is recalling reprocessed BARD Dynamic XT Deca Steerable catheters (Product Number 201102) used in electrophysiology procedures due to incomplete seals on the sterile packaging. The recall affects products distributed nationwide across the United States, as well as in Canada and Israel. This is classified as a Class II recall, indicating a potential health risk.
- Recalling firm
- Stryker Sustainability Solutions
- Product
- BARD Dynamic XT Deca Steerable, Product Number 201102, 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/383678da-1701-493b-b662-6d2f0f07575b