i-STAT EG6+ cartridge. List Number: 03P77-25.
This recall is currently active, issued September 17, 2025. It was issued by Abbott Point Of Care Inc..
- Company
- Abbott Point Of Care Inc.
- Recall Initiated
- August 21, 2025
- Posted
- September 17, 2025
- Recall Number
- Z-2585-2025
- Quantity
- 547,250 units
- Firm Location
- Princeton, NJ
- Official Source
- View on FDA website ↗
Reason for Recall
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Distribution
US Nationwide distribution.
Lot / Code Info
List Number: 03P77-25. All lot numbers.
Root Cause
No Marketing Application
Action Taken
Abbott notified consignees via email and letter on about 08/21/2025. Consignees were instructed to download, review and implement the updated i-STAT CG8+, EG7+ and EG6+ cartridge Instructions for Use (IFU), discontinue use of i-STAT CG8+, EG7+ and EG6+ cartridges for testing of capillary whole blood samples for potassium and ionized calcium, and use venous or arterial whole blood or an alternate method for testing capillary potassium and ionized calcium. Update the pH and PO2 reportable ranges on the i-STAT 1 analyzers running i-STAT CG8+, EG7+ or EG6+ cartridges. As 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) for more information. 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 CG8+, EG7+ or EG6+ cartridges to another facility, they were requested to notify them.