FDA Medical Device Recalls (openFDA)
Misys Healthcare Systems: Misys Commercial Laboratory version 2.x thru 3.4.1
- Recall number
- Z-0920-03
- Recalling firm
- Misys Healthcare Systems
- Product
- Misys Commercial Laboratory version 2.x thru 3.4.1
- Status
- Terminated
- Initiated
- 2003-04-01
- Posted
- 2003-06-05
- Terminated
- 2004-04-21
- Reason
- Urgent care STAT reports are not printing in a timely fashion.
- Root cause
- Other
- Action
- Recall notifications were sent to users on April 1, 2003 in Product Safety Notice PSN-03-L16 by facsimile.
- Quantity
- 109
- Distribution
- Nationwide and to Canada.
- Lot, serial or model codes
- Versions 2.x through 3.4.1
- 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