# FDA recall Z-0145-2024

> **Cardinal Health 200, LLC** · Class I · device recall initiated 2023-09-20.

## Product

Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack

## Reason for recall

Demonstrated recognition and compatibility issues with syringe infusion pumps.

## Distribution

US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.

## Key facts

- **Recall number:** Z-0145-2024
- **Recalling firm:** Cardinal Health 200, LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-20
- **Report date:** 2023-11-01

- **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-0145-2024

## Citation

> AI Analytics. FDA recall Z-0145-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0145-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
