Greiner Bio-One North America, Inc.: Medical Device Recall in 2021 - (Recall #: Z-2507-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 20, 2021

Date Posted: September 29, 2021

Recall Number: Z-2507-2021

Event ID: 88563

Reason for Recall:

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

Status: Terminated

Product Quantity: 956,400

Code Information:

Lot # B210533B Expiration 05/10/22 and B210439J Expiration 04/13/2022.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated