Misys Laboratory System, Versions 5.2, 5.23, 5.3 up to 5.3.2.
FDA device recall Z-0151-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Software defect causes orders to be lost under certain conditions of use. A typographical error at the Accept/Modfy/Reject prompt will cause the order not to be processed by the system.
- Action taken
- Product Safety Notice PSN-03-L32 was issued by fax to customers on July 7, 2003. It communcated a procedural workaround and that a follow-up notification was pending completion of a software engineering project to correct the defect.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 473
- Distribution
- Nationwide and to United Kingdom, Ireland, Denmark, Canada, Bermuda, Saudi Arabia, United Arab Emirates,
- Date initiated
- 2003-07-07
- Date posted
- 2004-07-20
- Date terminated
- 2004-09-23
- Location
- Tucson, AZ
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