Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry Recalled by Sunquest Information Systems, Inc. Due to The recall was initiated because Sunquest has confirmed...

Date: December 5, 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 Versions 6.4 and later using Microbiology Result Entry

Quantity: 127 sites

Why Was This Recalled?

The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory versions 6.4 and later while using Microbiology Result Entry (MRE), the specimen ribbon containing the Accession Number (AN) and the Battery Name may be missing or contain the wrong information.

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