Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Sunquest Encompass The reporting site is using the Encompass software Recalled by Sunquest Information Systems, Inc. Due to Sunquest is recalling the Sunquest Encompass versions 2.4...

Date: April 13, 2009
Company: Sunquest Information Systems, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Sunquest Information Systems, Inc. directly.

Affected Products

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

Quantity: 23 clients

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Sunquest Information Systems, Inc.

Sunquest Information Systems, Inc. has 9 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report