Reported May 20, 2026 · Ongoing
Daig Livewire Steerable, Product Number 401932; 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 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI 00885825007355
- Lot Numbers
393 of 393 codes
424806546259224792899488022949477224982083500492750220435031874506392642532534642049479861148802304950352498208950049305022044503222350639294253255464302248043754880231495094349820905008468502204550322255063931428243946508724804411488023349509454982091500847050220465032226506393243695594651469480495648803704950946498209350084995022051503222750639334386017465491248087554880374495094749820945008537502205250330285068012
- Amount recalled
- 458 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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