Stryker Sustainability Solutions: Catheter, Recording, Electrode, Reprocessed
Recall Summary Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable catheters (Product Number 6DYNTP001) due to incomplete seals on the sterile packaging. The affected products were distributed nationwide across the United States, as well as in Canada and Israel. This is a Class II recall, meaning the product could cause serious health problems or fail to work properly.
- Recalling firm
- Stryker Sustainability Solutions
- Product
- BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
- 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/cb3a234e-444e-465f-b0a1-9021eb8a18d5