Data Foundry

Medical device recalls 2014

DICOM Export Format for Sum Dose with Velocity v3 — Class II medical device recall Z-1275-2014

Terminated recall by Velocity Medical Solutions, LLC, reported 2014-04-02, distributed nationwide. An anomaly was detected such that, under certain conditions, a summed dose created by Velocity replaces the ca

Recall numberZ-1275-2014
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmVelocity Medical Solutions, LLC, Atlanta, GA, United States
Recall initiated2013-07-25
Classified2014-03-25
Reported by FDA2014-04-02
Terminated2014-09-11
DistributedNationwide (US)
Countries outside the USCH, IT
Quantity54 installs

Product

DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care specialists (physicians, physicists, dosimetrists, etc.) a means for comparison of medical imaging data from multiple DICOM conformant imaging modality sources. It allows the display, annotating, volume rendering, registration and fusing of medical images as an aid during use by diagnostic radiology, oncology, radiation therapy planning and other medical specialties.

Reason for recall

An anomaly was detected such that, under certain conditions, a summed dose created by Velocity replaces the calculated dose from an approved plan in Eclipse when importing the dose from Velocity.

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-1275-2014. 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.