# FDA recall Z-2375-2024

> **Greiner Bio-One North America, Inc.** · Class II · device recall initiated 2024-05-14.

## Product

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100  red cap-yellow ring, non-ridged

## Reason for recall

The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.

## Distribution

Nationwide Distribution to states of: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV and WY.

## Key facts

- **Recall number:** Z-2375-2024
- **Recalling firm:** Greiner Bio-One North America, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-14
- **Report date:** 2024-07-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Monroe, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2375-2024

## Citation

> AI Analytics. FDA recall Z-2375-2024. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-2375-2024. Source: US FDA. Licensed CC0.

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