Greiner Bio-One North America, Inc.: Medical Device Recall in 2020 - (Recall #: Z-1714-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 12, 2020

Date Posted: April 22, 2020

Recall Number: Z-1714-2020

Event ID: 85215

Reason for Recall:

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

Status: Terminated

Product Quantity: 1,000,800 units.

Code Information:

Item no. 454322. Lot no. B1908355. DI no. (01)29120017574488 (17) 200809 (10)B1908355.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated