Atlas FDA

Misys Laboratory System, version 5.3

FDA device recall Z-0926-03 · posted 2003-06-17 · Terminated

Recall details

Recalling firm
Misys Healthcare Systems
Reason for recall
Two clients reported Quality Assurance dates could not be entered after 5/19/03.
Action taken
Product Safety Notice number PSN-03-L24 was issued on May 13, 2003 to all affected customers. It contained an effective workaround and communicated that the software fix was available and also included that for those clients that wanted to install it. Clients are reminded to return acknowledgement cards included in the mailing.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
466
Distribution
Nationwide, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Kingdom, United Arab Emirates,
Date initiated
2003-05-13
Date posted
2003-06-17
Date terminated
2004-04-23
Location
Tucson, AZ

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