FDA Medical Device Recalls (openFDA)
Sunquest Information Systems: Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.
- Recall number
- Z-0325-03
- Recalling firm
- Sunquest Information Systems
- Product
- Misys Laboratory versions 5.2, 5.23, or 5.3 with ADT Interface to CoPathPlus.
- Status
- Terminated
- Initiated
- 2002-10-24
- Posted
- 2002-12-11
- Terminated
- 2013-02-26
- Reason
- Interfacing software systems have inconsistent character recognition characteristics.
- Root cause
- Other
- Action
- A recall notice was sent to hospitals on October 24, 2002. It communicated a temporary procedure to work around the problem. Also mentioned was the availabllity of a utility to detect and report suspected duplicate Medical Record Numbers.
- Quantity
- 190
- Distribution
- Nationwide and to Denmark, Bermuda, United Kingdom, Saudi Arabia, Canada.
- Lot, serial or model codes
- Versions 5.2, 5.23 and 5.3 with ADT Interface to CoPathPlus.
- 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