Misys Laboratory version 5.3
FDA device recall Z-0686-03 · posted 2003-04-02 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Patient results do not update properly when modified using on-line entry function.
- Action taken
- Product Safety Notice (PSN-03-L10) was sent to all affected clients by fax on 2/28/2003. It contained a procedural workaround. An announcement of the availability of a software upgrade or fix will be made when it is available.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 460
- Distribution
- Nationwide and to United Kingdom, Ireland, Denmark, Canada, Bermuda, Saudi Arabia, United Arab Emirates.
- Date initiated
- 2003-02-28
- Date posted
- 2003-04-02
- Date terminated
- 2004-06-02
- Location
- Tucson, AZ
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