Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and 3.4.2.
FDA device recall Z-1236-2009 · posted 2009-05-01 · Terminated
Recall details
- Recalling firm
- Cerner Corp
- Reason for recall
- Specimen labels printing incorrect patient demographics.
- Action taken
- 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
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 4
- Distribution
- Nationwide distribution to states of OH, NC, MO and MI.
- Date initiated
- 2009-01-19
- Date posted
- 2009-05-01
- Date terminated
- 2012-03-22
- Location
- Kansas City, MO
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