Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall 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

U.S. FDA — Device Enforcement · United States · 2021-12-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0502-2022
Date of alert
2021-12-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Greiner Bio-One North America, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
39120017579046
Reported risk: Some of the blood collection tubes show clotting due to variation of Lithium Heparin.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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