Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Abbott i-STAT CG8+ Cartridges intended for use in the in Recalled by Abbott Point Of Care Inc. Due to Inaccurate potassium results may be generated. When testing...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Abbott Point Of Care Inc. directly.
Affected Products
Abbott i-STAT CG8+ Cartridges intended for use in the in vitro quantification of potassium in arterial, venous, or capillary whole blood. List Number/UDI# : 03P88-25 ,(01)10054749000163(17)181028(10)L18059
Quantity: 17550 cartridges
Why Was This Recalled?
Inaccurate potassium results may be generated. When testing with control fluid and/or patient samples with low or reference range potassium concentration, elevated potassium results may be generated. When testing with samples with a high concentration of potassium, decreased potassium results may be generated
Where Was This Sold?
This product was distributed to 1 state: WI
About Abbott Point Of Care Inc.
Abbott Point Of Care Inc. has 28 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report