Atlas FDA

Mysys Laboratory System Version 5.3

FDA device recall Z-0972-03 · posted 2003-07-02 · Terminated

Recall details

Recalling firm
Misys Healthcare Systems
Reason for recall
Abnormal results are flagged as normal.
Action taken
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
Status
Terminated
Product code
JQP
Quantity affected
1
Distribution
Only to one hospital in Nebraska.
Date initiated
2003-03-19
Date posted
2003-07-02
Date terminated
2004-12-01
Location
Tucson, AZ

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