McKesson Radiology — Class II medical device recall Z-2872-2016
Terminated recall by Mckesson Medical Imaging Group, reported 2016-09-28, distributed in AK, AL, AR, AZ, CA, CO, FL, GA…. The STAT priority icon was not displayed in the Study List when the study was opened.
| Recall number | Z-2872-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Medical Imaging Group, Richmond, British Columbia, Canada |
| Recall initiated | 2016-07-12 |
| Classified | 2016-09-22 |
| Reported by FDA | 2016-09-28 |
| Terminated | 2019-11-20 |
| Distributed | 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 |
| Countries outside the US | CA, FR, GB, IE |
| Quantity | 164 devices |
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 for recall
The STAT priority icon was not displayed in the Study List when the study was opened.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2872-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.