ClearanceBrief
Recall Z-2346-2017 ยท JSP Kit, Anaerobic Identification

Biomerieux Inc

VITEK 2 Anaerobic and Corynebacteria identification card (ANC), REF 21347, 20 cards per carton.

DateMay 22, 2017 (initiated Apr 20, 2017)
StatusTerminated
ReasonThe integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Root causePackaging
ActionThe firm posted their recall notification on their customer website on 4/20/2017. The firm sent the recall notification letter to their customers via FedEx on 4/21/2017 for delivery 4/24/2017. A follow-up recall notice will be issued on 5/08/2017 which identified 3 additional lots impacted by the recall.
Quantity6316 cartons
DistributionNationwide distribution in the U.S, including military and government sites. The product was also distributed to Algeria, Angola, Argentina, Australia, Austria, Bahrain, Bangladesh, Belarus, Belgium, Bosnia - Herzegovina, Brazil, Brunei, Bulgaria, Burkina Faso, Cambodia, Cameroun, Canada, Chad, Ch
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.