Medical DevicesNationwide
BIOMERIEUX, INC. Bac T/ALERT 3D Control Module Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bac T/ALERT 3D Control Module
Brand
BIOMERIEUX, INC.
Lot Codes / Batch Numbers
All Models
Products Sold
All Models
BIOMERIEUX, INC. is recalling Bac T/ALERT 3D Control Module due to A Bac T/ALERT 3D system failed to detect a positive sample in a pediatric BAC T/ALERT PF bottle.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A Bac T/ALERT 3D system failed to detect a positive sample in a pediatric BAC T/ALERT PF bottle.
Recommended Action
Per FDA guidance
Consignees were notified by letter on May 27, 2005.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026