Mckesson Medical Imaging Group: Medical Device Recall in 2016 - (Recall #: Z-2872-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

McKesson Radiology, versions 12.1.1 and 12.2 McKesson Radiology (MR) is a Picture Archiving Communication System (PACS). It is a medical image and information management application that is intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from various medical imaging systems.

Product Classification:

Class II

Date Initiated: July 12, 2016

Date Posted: September 28, 2016

Recall Number: Z-2872-2016

Event ID: 75194

Reason for Recall:

The STAT priority icon was not displayed in the Study List when the study was opened.

Status: Terminated

Product Quantity: 164 devices

Code Information:

McKesson Radiology versions 12.1.1 and 12.2

Distribution Pattern:

Worldwide Distribution - US including AL, AK, AZ, AR, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, NE, NV, NH, NJ, NY, NC, OH, OK, PA, RI, SC, SD, TN, TX, VA, WA WV, WI, WY, and Internationally to Canada, France, Great Britain and Ireland

Voluntary or Mandated:

Voluntary: Firm initiated