RecallRadar

FDA Device recall Z-0750-2016

BacT/ALERT¿ FA, bioM¿rieux, Inc., Product Usage: BacT/ALERT¿ Culture Bottles are used with the BacT/ALERT¿ Microbial Detection System in qu…

On 2016-02-10 the FDA classified a Class II recall of BacT/ALERT¿ FA, bioM¿rieux, Inc., Product Usage: BacT/ALERT¿ Culture Bottles are used with the BacT/ALERT¿ Microbial Detection System in qu… by Biomerieux, citing bottles may have been exposed to non-normal shipping conditions which may lead to media degradation and impact growth performance.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0750-2016
ClassificationClass II
Statusterminated
Initiated2015-12-24
Published2016-02-10
Last updated2026-09-13 11:54 UTC
CompanyBiomerieux
Distributionn/a

Product

BacT/ALERT¿ FA, bioM¿rieux, Inc., Product Usage: BacT/ALERT¿ Culture Bottles are used with the BacT/ALERT¿ Microbial Detection System in qualitative procedures for enhanced recovery and detection of aerobic and facultative anaerobic microorganisms (bacteria and yeast).

Reason

Bottles may have been exposed to non-normal shipping conditions which may lead to media degradation and impact growth performance.

Identifiers

code_infoReference number: 259791, Lot number: 1042923, Expiry: 25JAN2016 and Lot number 1042979, Expiry: 28JAN2016.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0750-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.