ClearanceBrief
Recall Z-0859-2023 ยท JWY Manual Antimicrobial Susceptibility Test Systems

Biomerieux Inc

ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786

DateJan 4, 2023 (initiated Nov 9, 2022)
StatusOpen, Classified
ReasonAs the temperature and time out of range was exceeded, product performances cannot be guaranteed
Root causeStorage
ActionBiomerieux sent a FIELD SAFETY CORRECTIVE ACTION notice to the US subsidiary on 11/09/2022 by email. The notice requested the subsidiary identify their customers and issue an URGENT FIELD SAFETY NOTICE which explains the problem and request the following actions: "1. Confirm this letter has been distributed to and reviewed by all appropriate personnel within your organization. 2. Check your inventory for any of the impacted products (reference Table 1) associated with local shipments. 3. Stop using and scrap any remaining impacted products in your inventory. a. Request product replacement o
Quantity1 unit
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K010363ETEST MEROPENEM
Ab Biodisk, Apr 9, 2001