# FDA recall Z-1875-2025

> **Cardinal Health 200, LLC** · Class II · device recall initiated 2025-05-02.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-1875-2025
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-05-02
- **Report date:** 2025-06-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukegan, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1875-2025

## Citation

> AI Analytics. FDA recall Z-1875-2025. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1875-2025. Source: US FDA. Licensed CC0.

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