FDA Medical Device Recalls (openFDA)
Misys Healthcare Systems: Misys Laboratory System versions 5.2, 5.23 and 5.3
- Recall number
- Z-0626-03
- Recalling firm
- Misys Healthcare Systems
- Product
- Misys Laboratory System versions 5.2, 5.23 and 5.3
- Status
- Terminated
- Initiated
- 2003-01-31
- Posted
- 2003-03-06
- Terminated
- 2004-07-14
- Reason
- Software anomaly. Patient results may be filed in the incorrect patient file
- Root cause
- Other
- Action
- Notice of the correction was made by Fax on 1/31/2003. The notice indicated a procedural workaround to prevent the occurance of the defect. Corrections will be made to the software at only affected sites. These have been instructed to contact Applications Interface to schedule correction of the interface.
- Quantity
- 542
- Distribution
- Nationwide and to United Kingdom, Ireland, Belgium, Canada, Denmark, Bermuda, Saudi Arabia, United Arab Emirates,
- Lot, serial or model codes
- Versions 5.2, 5.23 and 5.3
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JQP
- Firm FEI
- 1000306472
- Firm city
- Tucson
- Firm state
- AZ
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28