Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FlexLab (FLX) Recalled by Inpeco S.A. Due to Module may freeze without generating user warning. There...
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 Inpeco S.A. directly.
Affected Products
FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2), Laboratory Automation System
Quantity: 18
Why Was This Recalled?
Module may freeze without generating user warning. There is a potential risk in delay of sample processing, leading to delayed delivery of test results to patients.
Where Was This Sold?
This product was distributed to 2 states: IL, NY
About Inpeco S.A.
Inpeco S.A. has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report