Sunquest Information Systems, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2272-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Sunquest Laboratory LabAccess Results Workstation (LARS)

Product Classification:

Class II

Date Initiated: October 5, 2010

Date Posted: September 5, 2012

Recall Number: Z-2272-2012

Event ID: 62714

Reason for Recall:

The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results.

Status: Terminated

Product Quantity: 151 sites

Code Information:

Sunquest Laboratory versions 5.3.3 and 6.3.0 SP3

Distribution Pattern:

Worldwide Distribution, including Nationwide (USA) and the countries of Canada, Denmark, Ireland, the United Arab Emirates and the United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated