Misys Laboratory System versions 5.23 and 5.3
FDA device recall Z-0804-03 · posted 2003-05-09 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Software anomaly.
- Action taken
- The firm sent notification of the situation in Product Safety Notice PSN-03-L14 by fax on 3/27/2003. It communicated a workaround solution and informed of an impending code addition intended to be made available at a future date.
- Root cause
- Other
- Status
- Terminated
- Quantity affected
- 463
- Distribution
- Nationwide and to United Kingdom, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates,
- Date initiated
- 2003-03-27
- Date posted
- 2003-05-09
- Date terminated
- 2004-04-21
- Location
- Tucson, AZ
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