Sunquest Information Systems, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2243-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting.

Product Classification:

Class III

Date Initiated: April 13, 2009

Date Posted: August 29, 2012

Recall Number: Z-2243-2012

Event ID: 62751

Reason for Recall:

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.

Status: Terminated

Product Quantity: 23 clients

Code Information:

versions 2.4 and later

Distribution Pattern:

Worldwide distribution: USA (nationwide) and country of: Bahamas.

Voluntary or Mandated:

Voluntary: Firm initiated