Class III — Low Risk

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

Sunquest Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: Recalled by Sunquest Information Systems, Inc. Due to In GUI inquiry, searching by ID (CID) may...

Date: August 12, 2011
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 Laboratory SMART & Sunquest Laboratory SMART Select Product Usage: for clinical use

Quantity: 47 sites

Why Was This Recalled?

In GUI inquiry, searching by ID (CID) may return the wrong patient demographic data if the accession number associated to the CID is no longer inactive.

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