BIOMERIEUX VIDAS 3, Compact immunoanalyzer with full traceability and automation
FDA Recall Z-0928-2020 · Posted None
Recalling FirmBiomerieux Inc
Recall StatusTerminated
Product CodeJJE
Date Initiated2019-10-22
Date Terminated2024-08-06
Product Quantity738 units
Reason for Recall
Following Customers complaints, investigations have been initiated on potentially false results obtained on VIDAS 3 with an expired calibration.
Indeed, the calibrations of assays were valid in the calibration menu whereas in fact the calibrations were expired and no alarm displayed to warn the users about the expiration date of the calibrations. Software computes results of analysis for assays with expired calibrations.
The anomaly is due to an incorrect update of the calibration status by the software.
Firm Action
The firm initiated their field action by an email to their subsidiaries on 10/22/2019. The subsidiaries then notified their customers by 2-day express via Fed Ex. In the US customer letter, customers are instructed to check their software version. If the VIDAS 3 software version is between 1.2.0 and 1.3.1, customers are instructed to check the archiving mode. If the archiving mode is Automatic When Results are Reported then customers are instructed how to configure the workaround, and to contact bioMerieux if the customer has the incorrect software configuration. bioMerieux then instructs impacted customers to review and interpret results in the context of the overall clinical procedure. Once this is completed to complete the acknowledgment form in Attachment A and return it the local bioMerieux representative and confirm receipt of this notice.
Root Cause
Software design
Distribution Pattern
US
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.