Cardinal Health 200, LLC: Medical Device Recall in 2025 - (Recall #: Z-1875-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Catalog No. 8888160648; Umbilical Vessel Catheter 5 French triple lumen

Product Classification:

Class II

Date Initiated: May 2, 2025

Date Posted: June 4, 2025

Recall Number: Z-1875-2025

Event ID: 96783

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.

Status: Ongoing

Product Quantity: 2280

Code Information:

UDI-DI (ea) 10192253040371; UDI-DI (box) 50192253040379 Lots 2419800006 2335500149

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated