Reported May 20, 2026 · Ongoing
Medtronic Marinr Steerable, Product Number 72402; 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?
- Medtronic Marinr Steerable, Product Number 72402; REPROCESSED ELECTROPHYSIOLOGY CATHETER
- Lot codes and dates
- UDI00885825011260
- Lot Numbers
66 of 66 codes
414788147600914848398496619249950025022496505358044701184778468484897649661934999115502936250635864490754479680048552944966194500256550293635068369450900948151214866012496619550025665029364507646445278834815122487414949691325002873502953550853374655115482015148833544973129500939250296985085818472048448267774890964498109950148185032181473076248450604940777498241850176005032182475487648468534941142498751650181805039989
- Amount recalled
- 87 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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