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

Recall Z-2297-2019 — BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes, Catalog Number 366667

U.S. FDA — Device Enforcement · United States · 2019-06-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2297-2019
Date of alert
2019-06-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Company
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
30382903666677
Reported risk: False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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