Reported May 20, 2026 · Ongoing
Daig Livewire Steerable, Product Number 401915; 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?
- Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI 00885825007300
- Lot Numbers
193 of 193 codes
177260739941384539200480844449859245010522504294224829524046485453920648086774986242501052450429442521570416402045404764812775498624350179095042945252163641665704544644481788849862445018848504388125216604182322454945248240894986245502013550438832577590418317645494584824092498625650201365052391271187742065844549460482409349863995020139505658027694034216286455186348255614993904502014750601522769695424757745677364830114
- Amount recalled
- 206 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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