FDA Recall Terminated

Misys Laboratory System version 5.3

Recall: Z-0807-03 · Initiated April 1, 2003

Recall

Recall Number
Z-0807-03
Event Number
26045
Firm
Misys Healthcare Systems
FEI Number
1000306472
Status
Terminated
Root Cause
Other
Initiated
April 1, 2003
Posted
May 9, 2003
Terminated
April 21, 2004
Address
4801 E Broadway Blvd, Tucson, AZ, 85711

Description

Misys Laboratory System version 5.3

Reason

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

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.

Distribution

States of MI, OH, NY.

Quantity

3