Reported Jun 4, 2025 · Ongoing
Catalog No. 8888160333; Umbilical Vessel Catheter 3.5 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. 8888160333; Umbilical Vessel Catheter 3.5 French single lumen
- Lot codes and dates
- UDI-DI (ea) 10192253040302; UDI-DI (box) 50192253040300 Lots
24313001572431300158243130015624313001542431300153243330019724313001522418100101243330020024183000642432300069241700011524318001392432200143243260025124170001162433300199241810010324323000662418300063243330019524326002502430300087243330019324303000852417000113243330020124322001392429900138241230000424303000832430300086243030008424181001022431300155
- UDI-DI (ea) 10192253040302; UDI-DI (box) 50192253040300 Lots
- Amount recalled
- 58742
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.
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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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