Stryker Sustainability Solutions 2026-05-20 Health serious FDA
Health · FDA · Recall #FDA-Z-2174-2026
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER Recall
Issued May 20, 2026 · Stryker Sustainability Solutions
In May 2026, Stryker Sustainability Solutions recalled the BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Incomplete seals on sterile product
What you should do
- 1 Stop using BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Stryker Sustainability Solutions to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Stryker Sustainability Solutions
- Category
- Health
- Recall date
- May 20, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide and the countries of Israel and Canada.
- Recall number
- FDA-Z-2174-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Stryker Sustainability Solutions has 6 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.