Product Safety Recalls

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Biomerieux Inc Recall 91148

Description: ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449

Biomerieux Inc Recall 91148 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0829-2023
Event ID91148
Event DescriptionETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449
Product TypeDevices
DistributionUS Nationwide distribution.
Quantity2 units
Recall ReasonAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
Device Classification20230111
Device Code InfoUDI/DI 03573026378592, Batch Numbers: 1009190620
Center Classification Date20230104
Recall Initiation Date20221109
Recalling FirmBiomerieux Inc
Initial Notification E-Mail
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