Product Wiki · Recalls · U.S. FDA — Device Enforcement

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 (physicians, physicists, dosimetrists, etc.) a means for comparison of medical imaging data from multiple DICOM conformant imaging modality sources. It allows the disp

U.S. FDA — Device Enforcement · United States · 2013-07-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1275-2014
Date of alert: 2013-07-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Velocity Medical Solutions, LLC
Product category: device
Product type: Devices

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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