Calculator/ Data Processing Module for Clinical Use.
FDA device recall Z-0235-04 · posted 2003-12-18 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Software Defect. When orders are modified before the Roche Cobas Integra query for a specimen, the sample ID locks.
- Action taken
- Firm has issued notifcation to all affected customers.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 485
- Distribution
- US, UK, Ireland, Denmark, Canada, Bermuda, Saudi Arabia and United Arab Emirates
- Date initiated
- 2003-09-25
- Date posted
- 2003-12-18
- Date terminated
- 2004-09-03
- Location
- Tucson, AZ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.