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

Recall Z-0159-2016 — CC cartridges for IRMA TRUPOINT Blood Gas Analyzer, PN 039903. The CC Cartridge are single use, disposable, in vitro diagnostics intended for point of care (POC), professional, use with the IRMA TRUpoint¿ Blood Analysis System.

U.S. FDA — Device Enforcement · United States · 2015-09-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0159-2016
Date of alert
2015-09-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
LifeHealth, LLC
Product category
device
Product type
Devices
Reported risk: May report values outside the published performance specifications for pH. After a certain point in shelf life, the pH sensor may give results that are falsely elevated. The discrepancy is greater as shelf life progresses and can be seen on the aqueous controls before the blood.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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