Reported May 20, 2026 · Ongoing
BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Stryker Sustainability Solutions
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Sustainability Solutions · 1810 W Drake Dr · Tempe, AZ · 85283-4327
Is this the product you have?
- BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI 00885825002930
- Lot Numbers
396609743142544490535451136745176324607771476268840564914401626449054045113684567842462822947753094137164445538344905424511369456784446282324875058415402444630334490544451137045678664628234502328441651784472622449580745113724567888462824250232854250497449053345020164511375456789846657675069705430058644905344511155451400446077454762686
- Amount recalled
- 61 units
This recall covers 26 products
The agency filed one notice per product. You are reading one of them; the other 25 are below.
13 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Incomplete seals on sterile product
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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