[Recalled] Sunquest Encompass The reporting site is using the Encompass software in an acute patient care setting. — Sunquest is recalling the Sunquest Encompass versions 2.4 and later because the… | FDA 2009-04-13

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: 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.

This Class III recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Sunquest Information Systems, Inc.

• Sunquest Laboratory : intended for use by professionals working in a clinical laboratory. — Class III
• Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: for clinical use — Class III
• Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry — Class II
• Sunquest Laboratory LabAccess Results Workstation (LARS) — Class II
• Sunquest Laboratory Sunquest Laboratory is intended for use by professionals working in a clinical laboratory. Sunquest Laboratory is intended for use only by professionals who have received extensive training in the use of the software. Sunquest Laboratory is controlled via userdefined security — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.