RecallRadar

FDA Device recall Z-1275-2014

DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care specialists (physicia…

On 2014-04-02 the FDA classified a Class II recall of DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care specialists (physicia… by Velocity Medical Solutions, citing 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 dos….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1275-2014
ClassificationClass II
Statusterminated
Initiated2013-07-25
Published2014-04-02
Last updated2026-09-13 11:53 UTC
CompanyVelocity Medical Solutions
DistributionUS

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

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.

Identifiers

code_infoVelocityAIS 3.0.0

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1275-2014%22

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