Atlas FDA

Misys Laboratory System version 5.3

FDA device recall Z-1092-03 · posted 2003-08-07 · Terminated

Recall details

Recalling firm
Misys Healthcare Systems
Reason for recall
Patient files become mixed up due to a software defect.
Action taken
Client was faxed a notice. All duplicate order numbers were identified, corrected and resent to the hospital system.
Root cause
Other
Status
Terminated
Product code
JQP
Quantity affected
1
Distribution
Only to Memorial-Sloan-Kettering Cancer Center, New York, NY.
Date initiated
2003-07-02
Date posted
2003-08-07
Date terminated
2004-04-23
Location
Tucson, AZ

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