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FDAFDA · Food and drugs·Recall number Z-2243-2012

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

Published August 29, 2012 · Recall initiated: April 13, 2009

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Sunquest Information Systems, Inc.
Distributor
Worldwide distribution: USA (nationwide) and country of: Bahamas.
Lot
versions 2.4 and later
Risk classification
Class III
Area (FDA)
device
Country
United States

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