Misys Laboratory System versions 5.2, 5.23 and 5.3
FDA device recall Z-0626-03 · posted 2003-03-06 · Terminated
Recall details
- Recalling firm
- Misys Healthcare Systems
- Reason for recall
- Software anomaly. Patient results may be filed in the incorrect patient file
- Action taken
- Notice of the correction was made by Fax on 1/31/2003. The notice indicated a procedural workaround to prevent the occurance of the defect. Corrections will be made to the software at only affected sites. These have been instructed to contact Applications Interface to schedule correction of the interface.
- Root cause
- Other
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 542
- Distribution
- Nationwide and to United Kingdom, Ireland, Belgium, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates,
- Date initiated
- 2003-01-31
- Date posted
- 2003-03-06
- Date terminated
- 2004-07-14
- Location
- Tucson, AZ
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