FDA Recall Open, Classified

i-STAT CG4+ cartridge (white). List Number: 03P85-25.

Recall: Z-2582-2025 · Initiated August 21, 2025

Recall

Recall Number
Z-2582-2025
Event Number
97442
Firm
Abbott Point Of Care Inc.
FEI Number
2245578
Product Code
CHL
Status
Open, Classified
Root Cause
No Marketing Application
Initiated
August 21, 2025
Posted
September 17, 2025
Address
400 College Rd E, Princeton, NJ, 08540-6607

Description

i-STAT CG4+ cartridge (white). List Number: 03P85-25.

Reason

Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.

Action

Abbott notified consignees via email and letter on about 08/21/2025. Consignees were instructed to download, review and implement the updated i-STAT CG4+ cartridge Instructions for Use (IFU), discontinue use of the i-STAT CG4+ cartridges for testing of capillary whole blood samples for lactate and instead use venous or arterial whole blood or an alternate method for testing capillary whole blood for lactate, and update the pH and PO2 reportable ranges on the i-STAT 1 analyzers running i-STAT CG4+ cartridges. This feature is not customizable through the i-STAT 1 handheld keypad, please see the i-STAT DE Quick Reference Guide - Customizing Reportable Ranges (ART 770547-00 Revision A). To use the Custom Reportable Range feature, you must have the i-STAT 1 handheld and i-STAT DE version 2.3 or higher. Changes to the reportable range may require a change to the Laboratory Information System (LIS) interface. Additionally, consignees were requested to confirm receipt and understanding of this communication by responding to the business reply card included with the letter. If consignees have forwarded any i-STAT CG4+ cartridges to another facility, they were requested to notify them.

Distribution

US Nationwide distribution.

Quantity

9,067,050 units