Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.
FDA device recall Z-0867-03 · posted 2003-05-29 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Incorrect results could be filed.
- Action taken
- The firm sent Product Safety Notice PSN-03-L18 by fax to customers on 4/14/2003.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 193
- Distribution
- Nationwide and to Ireland, Canada, Denmark, United Kingdom, Saudi Arabia, United Arab Emirates.
- Date initiated
- 2003-04-14
- Date posted
- 2003-05-29
- Date terminated
- 2004-04-21
- Location
- Tucson, AZ
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