Mysys Laboratory System Version 5.3
FDA Recall Z-0972-03 · Posted 2003-07-02
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Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-03-19
Date Terminated2004-12-01
Product Quantity1
Reason for Recall
Abnormal results are flagged as normal.
Firm Action
This is a completed recall. Consignee has had the software patch installed and reports it to be functional as of March 19, 2003. Recall notice was also sent that same day.
Root Cause
Other
Distribution Pattern
Only to one hospital in Nebraska.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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