RegWardenFDA facility compliance records
Recall

Class II — bioMerieux, Inc.

Recalling firmBIOMERIEUX SA
Registered facilityView this company's 16 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonBacT/ALERT SA Culture Bottle lot 1031866 may contain bottles with uncured sensors.
ProductBacT/ALERT SA Blood Culture Bottle. The BacT/ALERT SA reagent bottle is intended to be recover and detect aerobic microorganisms (bacteria and fungi) from blood and other normally sterile body fluids.
Quantity1690 cases
DistributionWorldwide Distribution.USA including the states of AR, AZ, CA, CO, DE, FL, GA, IL, IN, KY, LA, MD, MI, MN, MO, NC, NJ, NY, OH, OR, PA, RI, SC, SD, TN, TX, VA, WI, and WV, and the countries of China, Curacao and Japan.
Initiated2012-12-25
Classified2013-01-25
Terminated2014-06-03
Recall numberZ-0738-2013
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — bioMerieux, Inc. (Z-0738-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/64054/

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