# FDA recall Z-0502-2022

> **Greiner Bio-One North America, Inc.** · Class II · device recall initiated 2021-12-09.

## Product

greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P

## Reason for recall

Some of the blood collection tubes show clotting due to variation of Lithium Heparin.

## Distribution

Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA.  There was no foreign/military/government distribution.

## Key facts

- **Recall number:** Z-0502-2022
- **Recalling firm:** Greiner Bio-One North America, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-12-09
- **Report date:** 2022-01-26
- **Termination date:** 2023-10-10

- **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-0502-2022

## Citation

> AI Analytics. FDA recall Z-0502-2022. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0502-2022. Source: US FDA. Licensed CC0.

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