Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00 Recalled by Inpeco S.A. Due to The identified problem is an erroneous association between...
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 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00)is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation.
Quantity: 37 systems
Why Was This Recalled?
The identified problem is an erroneous association between the carrier and the sample tube caused by a communication error between the firmware of the Interface Modules and the Automation software. This problem can occur only when one of these Interface Modules is put off-line after a carrier in their secondary lane is physically returned on the main track and then put back on-line when the carrier is used to transport another tube.
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