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Terminated

Misys Laboratory System version 5.3

FDA Recall Z-1092-03 · Posted 2003-08-07

Recalling FirmMisys Healthcare Systems
Recall StatusTerminated
Product CodeJQP
Date Initiated2003-07-02
Date Terminated2004-04-23
Product Quantity1

Reason for Recall

Patient files become mixed up due to a software defect.

Firm Action

Client was faxed a notice. All duplicate order numbers were identified, corrected and resent to the hospital system.

Root Cause

Other

Distribution Pattern

Only to Memorial-Sloan-Kettering Cancer Center, New York, NY.

Official Source

View FDA Recall →

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

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