Health & Personal Care
HIGH
FDA DEVICE
Inpeco Recall: 8 FlexLab FLX Potassium Test System Units Over Unverified HIL Function (2025)
Inpeco recalled eight FlexLab FLX System Potassium Test System units sold in California and New York. The recall targets the Sample Integrity Module HIL function, which detects hemolysis, icterus and lipemia. The FDA has not evaluated this function for safety or effectiveness, risking erroneous results or delays. Labs should stop using the device immediately.
Inpeco
The FlexLab