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Terminated

Misys Laboratory System , Versions 5.2, 5.23 and 5.3

FDA Recall Z-0631-03 · Posted 2003-03-12

Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-02-07
Date Terminated2004-06-02
Product Quantity478

Reason for Recall

Missing patient data on Location Chart Copy Cumulative Reports.

Firm Action

Recall notice was faxed to customers on 2/7/2003. A software correction will be developed and another notice will be made that this is available.

Root Cause

Other

Distribution Pattern

Nationwide and to Bermuda, Canada, United Kingdom, Ireland, Denmark, Saudi Arabia, United Arab Emirates.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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