Date Initiated by Firm | February 19, 2003 |
Date Posted | March 21, 2003 |
Recall Status1 |
Terminated 3 on June 02, 2004 |
Recall Number | Z-0670-03 |
Recall Event ID |
25679 |
Product Classification |
Calculator/Data Processing Module, For Clinical Use - Product Code JQP
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Product | Misys Laboratory System Version 5.3 |
Code Information |
Version 5.3 |
Recalling Firm/ Manufacturer |
Misys Healthcare Systems 4801 E Broadway Blvd Tucson AZ 85711
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For Additional Information Contact | Mark Ellis 520-570-2000 |
Manufacturer Reason for Recall | Software anomaly. The HIDE command used to suppress suspected individual microbiology observations does not work in GUI inquiry |
FDA Determined Cause 2 | Other |
Action | Notification was made by FAX to customers. A procedureal work around was provided also. The firm will announce the availability of a software fix in the future. |
Quantity in Commerce | 464 |
Distribution | Nationwide and to United Kingdom, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates. |
Total Product Life Cycle | TPLC Device Report |
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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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