Greiner Bio-One North America, Inc.: Medical Device Recall in 2023 - (Recall #: Z-1583-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA, 13x100 pink cap-black ring, non-ridged, 24 racks of 50 pcs., 1200 pcs in total, Item #456003

Product Classification:

Class II

Date Initiated: March 31, 2023

Date Posted: May 24, 2023

Recall Number: Z-1583-2023

Event ID: 92025

Reason for Recall:

Some of the tubes may be incorrectly labeled.

Status: Completed

Product Quantity: 36,000 pieces (30 full cases)

Code Information:

Lot #B220533J, Exp. 2023-10-31, UDI Case label (01)39120017576496(17)231031(10)B220533J, UDI Rack label 29120017576499(17)231031(10)B220533J.

Distribution Pattern:

US Nationwide distribution in the states of WI and GA.

Voluntary or Mandated:

Voluntary: Firm initiated