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Terminated

Misys Laboratory System, Versions 5.2, 5.23, 5.3 up to 5.3.2.

FDA Recall Z-0151-04 · Posted 2004-07-20

Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-07-07
Date Terminated2004-09-23
Product Quantity473

Reason for Recall

Software defect causes orders to be lost under certain conditions of use. A typographical error at the Accept/Modfy/Reject prompt will cause the order not to be processed by the system.

Firm Action

Product Safety Notice PSN-03-L32 was issued by fax to customers on July 7, 2003. It communcated a procedural workaround and that a follow-up notification was pending completion of a software engineering project to correct the defect.

Root Cause

Other

Distribution Pattern

Nationwide and to United Kingdom, Ireland, Denmark, Canada, Bermuda, 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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