FDA Device recall Z-2872-2016
McKesson Radiology, versions 12.1.1 and 12.2 McKesson Radiology (MR) is a Picture Archiving Communication System (PACS). It is a medical im…
- FDA Device
- Class II
- terminated
- Published 2016-09-28
On 2016-09-28 the FDA classified a Class II recall of McKesson Radiology, versions 12.1.1 and 12.2 McKesson Radiology (MR) is a Picture Archiving Communication System (PACS). It is a medical im… by Mckesson Medical Imaging Group, citing the STAT priority icon was not displayed in the Study List when the study was opened.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2872-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-12 |
| Published | 2016-09-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Mckesson Medical Imaging Group |
| Distribution | AK, AL, AR, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NH, NJ, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, VA, WA, WI, WV, WY |
Product
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.
Reason
The STAT priority icon was not displayed in the Study List when the study was opened.
Identifiers
| code_info | McKesson Radiology versions 12.1.1 and 12.2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2872-2016%22
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