FDA Device recall Z-2243-2012
Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting
- FDA Device
- Class III
- terminated
- Published 2012-08-29
On 2012-08-29 the FDA classified a Class III recall of Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting by Sunquest Information Systems, citing sunquest is recalling the Sunquest Encompass versions 2.4 and later because the specimen collect time is displaying and printing one hour later than the actual collect time only w….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2243-2012 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2009-04-13 |
| Published | 2012-08-29 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sunquest Information Systems |
| Distribution | US |
Product
Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting.
Reason
Sunquest is recalling the Sunquest Encompass versions 2.4 and later because the specimen collect time is displaying and printing one hour later than the actual collect time only when Daylight Saving Time is active.
Identifiers
| code_info | versions 2.4 and later |
|---|
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-2243-2012%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.