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

Recall Z-1265-2020 — i-STAT G3+ cartridge (blue), List No. 03P78-50, UDI (01) 00054749002283 - Product Usage: The i-STAT G3+ cartridge may be used for the quantitative measurement of pH, pCO2, and pO2 in venous, arterial or capillary whole blood.

U.S. FDA — Device Enforcement · United States · 2020-01-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1265-2020
Date of alert
2020-01-14
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)
00054749002283
Reported risk: Marketed without a 510(k). Abbott Point of Care has determined that it does not have sufficient clinical evidence to fully characterize the performance of the blue i-STAT G3+ cartridges and therefore will no longer distribute the i-STAT G3+ (blue) cartridge in the United States as of May 1, 2020.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.