Bac T/ALERT 3D Control Module

This recall has been terminated (originally issued September 7, 2005).

Company: Biomerieux, Inc.
Recall Initiated: May 27, 2005
Posted: September 7, 2005
Terminated: September 21, 2006
Recall Number: Z-0612-05
Quantity: 744 units
Firm Location: Durham, NC
Official Source: View on FDA website ↗

Reason for Recall

A Bac T/ALERT 3D system failed to detect a positive sample in a pediatric BAC T/ALERT PF bottle.

Distribution

Nationwide, Argentina, Australia/N. Zealand, Austria, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, Finland, France, Germany, Greece, Hong Kong, India, Italy, Ivory Coast, Japan, Korea, Mexico, Netherlands, Norway, Poland, Portugal, Russia, Sweden, Switzerland, Turkey, UK