Sunquest Information Systems, Inc.: Medical Device Recall in 2012 - (Recall #: Z-0073-2013)

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 : intended for use by professionals working in a clinical laboratory.

Product Classification:

Class III

Date Initiated: November 15, 2011

Date Posted: October 24, 2012

Recall Number: Z-0073-2013

Event ID: 62516

Reason for Recall:

Online calculations may not be performed as expected or may yield results that are different than expected when the calculation module is called from the Online Entry (OEM) application for a subtest whose subcolumn number on the instrument online string is divisible by 10.

Status: Terminated

Product Quantity: 127 sites

Code Information:

Versions 6.4.0 and later

Distribution Pattern:

Nationwide distribution

Voluntary or Mandated:

Voluntary: Firm initiated