Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and 3.4.2.
FDA Recall Z-1236-2009 · Posted 2009-05-01
Recalling FirmCerner Corp
Recall StatusTerminated
Product CodeJQP
Date Initiated2009-01-19
Date Terminated2012-03-22
Product Quantity4
Reason for Recall
Specimen labels printing incorrect patient demographics.
Firm Action
Cerner Corporation issued a "Priority Review Flash" dated January 15, 2009 via e-mail to consignees using the software. The letter described the violative nature of the software and explained the proper navigation controls needed to prevent further issues.
Further questions should be addressed to Bridge Client Support at 1-800-786-0239.
Root Cause
Software design
Distribution Pattern
Nationwide distribution to states of OH, NC, MO and MI.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.