Reported May 20, 2026 · Ongoing
Daig Livewire Steerable, Product Number 401581; 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 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI 00885825006877
- Lot Numbers
69 of 69 codes
368385738368783981321404277840535854103495449689736838583891551399143440527214053586411121244968983694871393247039914394052723410347941112134549309376237539424623991442405272641034804111214454931237646053964790399144440527274103481411121645709263764606397186039914454052735410348241112184570936376757539737974042769405274741034834111219474979037679543981001404277340535794103491449688447532443769052398100540427764053580
- Amount recalled
- 108 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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