# FDA recall Z-1714-2020

> **Greiner Bio-One North America, Inc.** · Class II · device recall initiated 2020-03-12.

## Product

VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

## Reason for recall

Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate.

## Distribution

US nationwide distribution in the states of: NJ, IN, TN, MI, NC, WA, KS, CA, LA, IL, MD, NY, OH, TX, GA, KY, PA, CO, MA, PR, FL, AR, OK and NE.

## Key facts

- **Recall number:** Z-1714-2020
- **Recalling firm:** Greiner Bio-One North America, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-03-12
- **Report date:** 2020-04-22
- **Termination date:** 2022-08-31

- **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-1714-2020

## Citation

> AI Analytics. FDA recall Z-1714-2020. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-1714-2020. Source: US FDA. Licensed CC0.

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