Reported May 20, 2026 · Ongoing
BARD Dynamic Deca Steerable, Product Number 201101; 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 Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI 00885825003845
- Lot Numbers
2,614 of 2,614 codes
302165641583684305347445764045603834660045481549748815944987017503294231078694160047430534844579044562726466005248154994881600498701850336113171909416004843055004460044456514246622424816776488161349873555033612319766741600494305998446150545658974662243481689048816154989058503362632318454160051430799844615554565899466254648168914881618498906050336273241416416005343080044461558456590146625474816898488258549906295033628
- Amount recalled
- 3063 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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