Product Safety Recalls

Product Recall Tracker

Greiner Bio-One North America, Inc. Recall 89216

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

Greiner Bio-One North America, Inc. Recall 89216 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0502-2022
Event ID89216
Event Descriptiongreiner 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 TypeDevices
DistributionDistribution was made to FL, IL, MO, NC, NM, NY, PA, TN, TX, and VA. There was no foreign/military/government distribution.
Quantity889,200 pcs.
Recall ReasonSome of the blood collection tubes show clotting due to variation of Lithium Heparin.
Device Classification20220126
Device Code InfoLot #B21053QG, Exp. 09/09/2022, UDI: Case: 39120017579046, Rack: 29120017579049.
Center Classification Date20220118
Recall Initiation Date20211209
Recalling FirmGreiner Bio-One North America, Inc.
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.