Data Foundry

Medical device recalls 2014

Horizon Medical Imaging It is a medical image and information… — Class II medical device recall Z-2121-2014

Terminated recall by Mckesson Medical Immaging, reported 2014-08-06, distributed in AK, AL, AR, AZ, CA, CO, CT, FL…. The firm has identified a software issue which may cause a discrepancy between the index of images expected by

Recall numberZ-2121-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMckesson Medical Immaging, Richmond, British Columbia, Canada
Recall initiated2014-05-05
Classified2014-07-28
Reported by FDA2014-08-06
Terminated2017-04-13
DistributedAK, AL, AR, AZ, CA, CO, CT, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, VT, WA, WI, WV, WY
Countries outside the USAU, CA, FR, GB, IE
Quantity659 units
Reason classessoftware

Product

Horizon Medical Imaging 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 firm has identified a software issue which may cause a discrepancy between the index of images expected by the application, and the actual content of the folder storing the images.

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-2121-2014. 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.