Misys Laboratory System Versions 5.2, 5.23 and 5.3
FDA device recall Z-0614-03 · posted 2003-03-06 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Software anomaly. Rejecting the selected Autofiling status may result in the change being accepted rather than rejected.
- Action taken
- Firm sent notice by FAX on 1/31/2003. A workaround provided should prevent the problem until a software fix is made available. Clients can expect a notice when this is made available.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 542
- Distribution
- Nationwide and to United Kingdom, Canada, Denmark, Ireland, Bermuda, Saudi Arabia, United Arab Emirates.
- Date initiated
- 2003-01-31
- Date posted
- 2003-03-06
- Date terminated
- 2004-05-07
- Location
- Tucson, AZ
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