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Terminated

Misys Laboratory System version 5.3

FDA Recall Z-0807-03 · Posted 2003-05-09

Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Date Initiated2003-04-01
Date Terminated2004-04-21
Product Quantity3

Reason for Recall

Software anomally, One client reported patient tests and results are deleted when duplicate orders are placed.

Firm Action

Notice was sent by fax on 4/1/2003 under Product Safety Notice, PSN-03-L17. A code modification is yet to be released. Customers have been provided with a temporary workaround procedure.

Root Cause

Other

Distribution Pattern

States of MI, OH, NY.

Official Source

View FDA Recall →

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

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