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 Aliquoter Module (mALX) may generate secondary sample...
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); Version: FLX-217-40;
Quantity: 14 units (1 US, 13 OUS)
Why Was This Recalled?
The Aliquoter Module (mALX) may generate secondary sample tubes without labels or with mismatched labels which may result in delayed results or erroneous results, this error occurs if the operators open the printer head of mALX to perform error recoveries or maintenance procedures and do not empty the printer tubes buffer to remove all the secondary sample tubes
Where Was This Sold?
This product was distributed to 1 state: MI
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