# FDA recall Z-2507-2021

> **Greiner Bio-One North America, Inc.** · Class II · device recall initiated 2021-08-20.

## Product

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged

## Reason for recall

Complaint of tubes clotting due to variation of anticoagulant and/or tubes have low vacuum.

## Distribution

US Nationwide distribution in the states of AL, AZ, CA, CT, FL, GA, IL, IN, KY, LA, MD, ME, MO, MT, NC, NE, NM, NV, NY, OH, OR, PA, TX, VA, WA and Puerto Rico.

## Key facts

- **Recall number:** Z-2507-2021
- **Recalling firm:** Greiner Bio-One North America, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-20
- **Report date:** 2021-09-29
- **Termination date:** 2023-10-04

- **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-2507-2021

## Citation

> AI Analytics. FDA recall Z-2507-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2507-2021. Source: US FDA. Licensed CC0.

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