# FDA recall Z-1583-2023

> **Greiner Bio-One North America, Inc.** · Class II · device recall initiated 2023-03-31.

## Product

greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003

## Reason for recall

Some of the tubes may be incorrectly labeled.

## Distribution

US Nationwide distribution in the states of WI and GA.

## Key facts

- **Recall number:** Z-1583-2023
- **Recalling firm:** Greiner Bio-One North America, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2023-03-31
- **Report date:** 2023-05-24

- **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-1583-2023

## Citation

> AI Analytics. FDA recall Z-1583-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1583-2023. Source: US FDA. Licensed CC0.

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