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FDA (Device enforcement)Recalled 2025-05-02class ii

Cardinal Health 200, LLC: Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen

Hazard

Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates.

Details from the source

Reason for recall: Packaging defect may compromise sterility of the product. Use of a non-sterile product on the patient could lead to infection in neonates. Distribution: Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, OR, PA, PR, RI, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Brazil, Canada, Chile, Colombia, Singapore, South Africa. Quantity: 2280 Lot/code info: UDI-DI (ea) 10192253040371; UDI-DI (box) 50192253040379 Lots 2419800006 2335500149

UPC codes

10192253040371, 50192253040379

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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