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Greiner Bio-One North America, Inc. Recall 88511

Description: VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

Greiner Bio-One North America, Inc. Recall 88511 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-2485-2021
Event ID88511
Event DescriptionVACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged
Product TypeDevices
DistributionDistribution was made to AL, AZ, CO, CT, FL, IL, MA, MD, MI, MO, NC, NM, PA, TX, and VA. Foreign distribution was made to Canada.
Quantity962,400 tubes
Recall ReasonBlood collection tubes may experience a clotting issue.
Device Classification20211006
Device Code InfoItem Number 456279, Lot B21033DA, exp. 09/08/2022, UDI Case - 39120017571248; UDI Rack - 29120017571241 UPDATE per 9/10/2021 email: Item Number 456279, Lot B21053R8, exp. 11/10/2022, UDI Case -39120017571248; UDI Rack - 29120017571241.
Center Classification Date20210924
Recall Initiation Date20210813
Recalling FirmGreiner Bio-One North America, Inc.
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