Reported Jun 4, 2025 · Ongoing
Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen
Cardinal Health 200, LLC
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: Cardinal Health 200, LLC · 3651 Birchwood Dr · Waukegan, IL · 60085-8337
Is this the product you have?
- Catalog No. 8888160341; Umbilical Vessel Catheter 5 French single lumen
- Lot codes and dates
- UDI-DI (ea) 10192253040319; UDI-DI (box) 50192253040317 Lots
242770015824256000662433000005242770016024256000672425600070241510011324256000712427700159241510011024121000932433000095242560006924256000772415100116242560006324256000742415100115241510011424121000962425600072242560007524044000612425600064241510010624256000762415100107241510011224256000732425600065240440006224044000652415100093241510010924151001112433000094
- UDI-DI (ea) 10192253040319; UDI-DI (box) 50192253040317 Lots
- Amount recalled
- 51378
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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