Misys Laboratory System version 5.3
FDA device recall Z-0807-03 · posted 2003-05-09 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Software anomally, One client reported patient tests and results are deleted when duplicate orders are placed.
- Action taken
- Notice was sent by fax on 4/1/2003 under Product Safety Notice, PSN-03-L17. A code modification is yet to be released. Customers have been provided with a temporary workaround procedure.
- Root cause
- Other
- Status
- Terminated
- Quantity affected
- 3
- Distribution
- States of MI, OH, NY.
- Date initiated
- 2003-04-01
- Date posted
- 2003-05-09
- Date terminated
- 2004-04-21
- Location
- Tucson, AZ
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