i-STAT EG7+ Cartridge (Abbott) – Sample Type Issue (2025)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
i-STAT EG7+ cartridge. List Number: 03P76-25.
Brand
Abbott Point Of Care Inc.
Lot Codes / Batch Numbers
List Number: 03P76-25. All lot numbers.
Products Sold
List Number: 03P76-25. All lot numbers.
Abbott Point Of Care Inc. is recalling i-STAT EG7+ cartridge. List Number: 03P76-25. due to 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 an. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026