Sunquest Information Systems, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2270-2012)

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 Versions 6.4 and later using Microbiology Result Entry

Product Classification:

Class II

Date Initiated: December 5, 2011

Date Posted: September 5, 2012

Recall Number: Z-2270-2012

Event ID: 62708

Reason for Recall:

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.

Status: Terminated

Product Quantity: 127 sites

Code Information:

Versions 6.4 and later

Distribution Pattern:

Worldwide Distribution -- USA (nationwide) and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated