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 The Firmware (FW) of the Automation System Interface...
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). (Different brand names of same product.)
Quantity: 262 total, 52 US
Why Was This Recalled?
The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur XP/XPT may lead to an incorrect association of test results to sample ID. Improper management of the sample may bring an incorrect patient result.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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