Inpeco S.A. Recalls

2 recalls found for Inpeco S.A.. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Inpeco S.A. Recalls Potassium Test System Over Safety Concerns

Inpeco S.A. recalled eight units of its FlexLab (FLX) Potassium Test System on September 3, 2025. The system's Sample Integrity Module may produce erroneous results due to unverified functions. Healthcare providers must stop using the device immediately and follow the manufacturer's instructions.

Inpeco S.A.
The FlexLab
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Health & Personal Care
HIGH
FDA DEVICE

Inpeco S.A. Recalls FlexLab X System Over Erroneous Test Results

Inpeco S.A. recalled one unit of the FlexLab X (FXX) System on September 3, 2025. The recall affects the Sample Integrity Module, which has not been FDA evaluated for safety. This may cause erroneous results or delays in patient testing.

Inpeco S.A.
The FlexLab
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Brand Statistics

Total Recalls
2
Pages
1

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