Misys Laboratory System versions 5.2, 5.23, 5.3, 5.3.1 and 5.3.2.
FDA Recall Z-0867-03 · Posted 2003-05-29
Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-04-14
Date Terminated2004-04-21
Product Quantity193
Reason for Recall
Incorrect results could be filed.
Firm Action
The firm sent Product Safety Notice PSN-03-L18 by fax to customers on 4/14/2003.
Root Cause
Other
Distribution Pattern
Nationwide and to Ireland, Canada, Denmark, United Kingdom, Saudi Arabia, United Arab Emirates.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.