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
    • 2427700158
    • 2425600066
    • 2433000005
    • 2427700160
    • 2425600067
    • 2425600070
    • 2415100113
    • 2425600071
    • 2427700159
    • 2415100110
    • 2412100093
    • 2433000095
    • 2425600069
    • 2425600077
    • 2415100116
    • 2425600063
    • 2425600074
    • 2415100115
    • 2415100114
    • 2412100096
    • 2425600072
    • 2425600075
    • 2404400061
    • 2425600064
    • 2415100106
    • 2425600076
    • 2415100107
    • 2415100112
    • 2425600073
    • 2425600065
    • 2404400062
    • 2404400065
    • 2415100093
    • 2415100109
    • 2415100111
    • 2433000094
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.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.