PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: April 22, 2020 Initiated: March 12, 2020 #Z-1714-2020

Product Description

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.

Details

Units Affected
1,000,800 units.
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.
Location
Monroe, NC

Frequently Asked Questions

What product was recalled?
VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.. Recalled by Greiner Bio-One North America, Inc.. Units affected: 1,000,800 units..
Why was this product recalled?
Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 22, 2020. Severity: Moderate. Recall number: Z-1714-2020.