FDA Device recall Z-0250-2013
Sunquest Laboratory, version 7.0 not available
- FDA Device
- Class II
- terminated
- Published 2012-11-14
On 2012-11-14 the FDA classified a Class II recall of Sunquest Laboratory, version 7.0 not available by Sunquest Information Systems, citing sunquest is recalling Sunquest Laboratory version 7.0 because when saving an Accession to a non-current Episode/Event, a User-Defined field can be incorrectly replaced by the curr….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0250-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2011-11-03 |
| Published | 2012-11-14 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sunquest Information Systems |
| Distribution | US |
Product
Sunquest Laboratory, version 7.0 not available
Reason
Sunquest is recalling Sunquest Laboratory version 7.0 because when saving an Accession to a non-current Episode/Event, a User-Defined field can be incorrectly replaced by the current Episode/Event User-Defined data.
Identifiers
| code_info | not available |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0250-2013%22
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