FDA Device recall Z-2272-2012
Sunquest Laboratory LabAccess Results Workstation (LARS)
- FDA Device
- Class II
- terminated
- Published 2012-09-05
On 2012-09-05 the FDA classified a Class II recall of Sunquest Laboratory LabAccess Results Workstation (LARS) by Sunquest Information Systems, citing the recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly comb….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2272-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2010-10-05 |
| Published | 2012-09-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sunquest Information Systems |
| Distribution | US |
Product
Sunquest Laboratory LabAccess Results Workstation (LARS)
Reason
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results.
Identifiers
| code_info | Sunquest Laboratory versions 5.3.3 and 6.3.0 SP3 |
|---|
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-2272-2012%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.