Skip to the content

FDA Medical Device Recalls (openFDA)

Sunquest Information Systems, Inc.: Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting.

Recall number
Z-2243-2012
Recalling firm
Sunquest Information Systems, Inc.
Product
Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting.
Status
Terminated
Initiated
2009-04-13
Posted
2012-08-22
Terminated
2012-08-22
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.
Root cause
Software design
Action
The firm, Sunquest, sent a "Urgent-Product Safety Notice: PSN-09-01" letter dated April 13, 2009 all their customers who purchase the Sunquest Encompass versions 2.4 and later. The letter informed the customers of the problem identified and the action to be taken. Customers were instructed to request software correction and to create a service request via client support webpage at www.sunquestinfo.com/supportweb. Then choose Submit a Service Request. Select Issue Type and select Software Request. When Software Request is selected, the Work Queue field automatically fills in with "Software Request." Promptly advise appropriate personnel. Customers with questions can contact Client Support and Services at (877) 239-6337 for US and Canadian sites and at +44(0)0800-960-972 for international sites.
Quantity
23 clients
Distribution
Worldwide distribution: USA (nationwide) and country of: Bahamas.
Lot, serial or model codes
versions 2.4 and later
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

Search this register