Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-0972-03

Mysys Laboratory System Version 5.3

CliniSys, Inc / initiated 2003-03-19 / Terminated

Misys Healthcare Systems began a recall of Mysys Laboratory System Version 5.3 on . The reason FDA records is "Abnormal results are flagged as normal". As of , the recall status on record is Terminated.

Recall record

Recall number
Z-0972-03
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
CliniSys, Inc
Product
Mysys Laboratory System Version 5.3
Product code
JQP Calculator/Data Processing Module, For Clinical Use
Reason for recall
Abnormal results are flagged as normal.
FDA root cause
Other
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.
Quantity in commerce
1
Distribution
Only to one hospital in Nebraska.
Product codes and lots
Version 5.3.