FDA Medical Device Recalls (openFDA)
Misys Healthcare Systems: Misys Laboratory System, version 5.3
- Recall number
- Z-0926-03
- Recalling firm
- Misys Healthcare Systems
- Product
- Misys Laboratory System, version 5.3
- Status
- Terminated
- Initiated
- 2003-05-13
- Posted
- 2003-06-17
- Terminated
- 2004-04-23
- Reason
- Two clients reported Quality Assurance dates could not be entered after 5/19/03.
- Root cause
- Other
- Action
- Product Safety Notice number PSN-03-L24 was issued on May 13, 2003 to all affected customers. It contained an effective workaround and communicated that the software fix was available and also included that for those clients that wanted to install it. Clients are reminded to return acknowledgement cards included in the mailing.
- Quantity
- 466
- Distribution
- Nationwide, Ireland, Canada, Denmark, Bermuda, Saudi Arabia, United Kingdom, United Arab Emirates,
- Lot, serial or model codes
- Version 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