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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