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U.S. Department of Health and Human Services

Class 2 Device Recall

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 Class 2 Device Recallsee related information
Date Initiated by FirmJuly 02, 2003
Date PostedAugust 07, 2003
Recall Status1 Terminated 3 on April 23, 2004
Recall NumberZ-1092-03
Recall Event ID 26784
Product Classification Calculator/Data Processing Module, For Clinical Use - Product Code JQP
ProductMisys Laboratory System version 5.3
Code Information Version 5.3
Recalling Firm/
Manufacturer		 Misys Healthcare Systems
4801 E Broadway Blvd
Tucson AZ 85711
For Additional Information ContactBarbara Brown
520-733-6403
Manufacturer Reason
for Recall		Patient files become mixed up due to a software defect.
FDA Determined
Cause 2		Other
ActionClient was faxed a notice. All duplicate order numbers were identified, corrected and resent to the hospital system.
Quantity in Commerce1
DistributionOnly to Memorial-Sloan-Kettering Cancer Center, New York, NY.
Total Product Life CycleTPLC 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.
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