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

Recall Z-1263-2020 — i-STAT CG4+ cartridge (blue), List No. 03P85-50. UDI (01) 00054749002269 - Product Usage: The i-STAT CG4+ cartridge is intended for the quantitative measurement of lactate, pH, pCO2, and pO2 in venous, arterial or capillary whole blood.

U.S. FDA — Device Enforcement · United States · 2020-01-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1263-2020
Date of alert
2020-01-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Abbott Point Of Care Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00054749002269
Reported risk: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not have CLIA waived status. CLIA recognizes two types of laboratory tests: waived and non-waived. Different CLIA standards apply to waived and non-waived tests as well as the facilities that perform these types of tests. The i-STAT CHEM8+ cartridge contains nine measured assays (sodium, potassium, chloride, blood urea nitrogen (BUN), ionized calcium, TCO2, glucose, creatinine and hematocrit) and is categorized as a CLIA waived test for venous whole blood samples, meaning this cartridge could be used in a facility with a CLIA Certificate of Waiver as a waived test.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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