Health & Personal Care
HIGH
FDA DEVICE
Inpeco FlexLab X System Potassium Test System Recalled for Unvalidated Hemolysis, Icterus, Lipemia H
The FlexLab X System Potassium Test System was recalled by Inpeco S.A. on 2025-09-03 after the FDA identified an unvalidated hemolysis, icterus, and lipemia function in its Sample Integrity Module. The recall affects US distribution to California and New York. Stop using immediately and follow manufacturer instructions.
Inpeco S.A.
The FlexLab