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U.S. Department of Health and Human Services

Class 2 Device Recall

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  Class 2 Device Recall see related information
Date Initiated by Firm February 07, 2003
Date Posted March 12, 2003
Recall Status1 Terminated 3 on June 02, 2004
Recall Number Z-0631-03
Recall Event ID 25624
Product Classification Calculator/Data Processing Module, For Clinical Use - Product Code JQP
Product Misys Laboratory System , Versions 5.2, 5.23 and 5.3
Code Information Versions 5.2, 5.23 and 5.3
Recalling Firm/
Misys Healthcare Systems
4801 E Broadway Blvd
Tucson AZ 85711
For Additional Information Contact Mark Ellis
Manufacturer Reason
for Recall
Missing patient data on Location Chart Copy Cumulative Reports.
FDA Determined
Cause 2
Action Recall notice was faxed to customers on 2/7/2003. A software correction will be developed and another notice will be made that this is available.
Quantity in Commerce 478
Distribution Nationwide and to Bermuda, Canada, United Kingdom, Ireland, Denmark, Saudi Arabia, United Arab Emirates.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.