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Terminated

Misys Laboratory System, version 5.3

FDA Recall Z-0926-03 · Posted 2003-06-17

Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-05-13
Date Terminated2004-04-23
Product Quantity466

Reason for Recall

Two clients reported Quality Assurance dates could not be entered after 5/19/03.

Firm Action

Product Safety Notice number PSN-03-L24 was issued on May 13, 2003 to all affected customers. It contained an effective workaround and communicated that the software fix was available and also included that for those clients that wanted to install it. Clients are reminded to return acknowledgement cards included in the mailing.

Root Cause

Other

Distribution Pattern

Nationwide, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Kingdom, 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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