FDAClass IIMay 24, 2023

greiner bio-one VACUETTE TUBE recall

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

Why was greiner bio-one VACUETTE TUBE recalled?

Some of the tubes may be incorrectly labeled.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
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
Recalling firm
Greiner Bio-One North America, Inc.
Quantity
36,000 pieces (30 full cases)
Distribution
US Nationwide distribution in the states of WI and GA.
Recall date
May 24, 2023
Classification
Class II
Status
Completed
Agency
FDA (device)
Open FDA enforcement record Latest recalls