Greiner Bio-One North America, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0502-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50 pcs., 1200 pcs. in total, REF 456087P

Product Classification:

Class II

Date Initiated: December 9, 2021

Date Posted: January 26, 2022

Recall Number: Z-0502-2022

Event ID: 89216

Reason for Recall:

Some of the blood collection tubes show clotting due to variation of Lithium Heparin.

Status: Terminated

Product Quantity: 889,200 pcs.

Code Information:

Lot #B21053QG, Exp. 09/09/2022, UDI: Case: 39120017579046, Rack: 29120017579049.

Distribution Pattern:

Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA. There was no foreign/military/government distribution.

Voluntary or Mandated:

Voluntary: Firm initiated