Cerner Corp Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and 3.4.2. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and 3.4.2.
Brand
Cerner Corp
Lot Codes / Batch Numbers
Software Versions 3.4.0, 3.4.1 and 3.4.2.
Products Sold
Software Versions 3.4.0, 3.4.1 and 3.4.2.
Cerner Corp is recalling Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and due to Specimen labels printing incorrect patient demographics.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Specimen labels printing incorrect patient demographics.
Recommended Action
Per FDA guidance
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.
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