FlexLab Automation System used with the following Modules: High Volume Storage(P/N FLX-270, FLX-271, FLX-276, FLX-282, FLX-283), HSQ Interface Module (P/N FLX-274), Aliquoter Module (P/N FLX-209), Rack Output Module ROM400 (P/N FLX-289), XN-9000 Interface Module (P/N FLX-290), Advia 2120 LAS Interface Module (P/N FLX-219), Vertical Transportation Module (P/N FLX -204), Rack Input Module (P/N FLX-214), AUWi System Interface Module (P/N FLX-286), Track To Rack Interface Module (P/N FLX-295) - Product Usage: 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.
FDA Recall Z-2114-2020 · Posted None
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Recalling FirmInpeco S.A.
Recall StatusTerminated
Product CodeCEM
Date Initiated2020-04-07
Date Terminated2024-06-13
Product Quantity10 systems
Reason for Recall
The sensors which activate the safety switches may be affected by delayed activation. In 1% of the cases, the response delay can be up to a maximum delay of 2 seconds, instead of 40ms
expected by design.
Firm Action
Urgent: Medical Device Correction notification letters dated 3/30/20 were sent to customers.
Action to be taken by the user
After module protection removal, wait at least 2 seconds before accessing the impacted module (listed in Table
1). Your service provider will contact you to replace the sensor. Until the service visit please maintain awareness on this notice.
Please complete and return the "Customer Letter Receipt Confirmation and Implementation Check form" attached to this letter within 15 days directly to the email address specified in the email communication.
Please transfer this notice to whom it might concern.
Contact reference person:
For any clarification you may need, do not hesitate to contact:
Eva Balzarotti - Regulatory Affairs Manager
E-mail: [email protected]
Phone: (+41) 919118 224
Root Cause
Component design/selection
Distribution Pattern
The products were distributed to the following US States: IL and NY.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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