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FDAFDA · Food and drugs·Recall number Z-0502-2022

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

Published January 26, 2022 · Recall initiated: December 9, 2021

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Greiner Bio-One North America, Inc.
Distributor
Distribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA. There was no foreign/military/government distribution.
Lot
Lot #B21053QG, Exp. 09/09/2022, UDI: Case: 39120017579046, Rack: 29120017579049.
Risk classification
Class II
Area (FDA)
device
Country
United States

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