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

Recall Z-1492-2017 — Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and e

U.S. FDA — Device Enforcement · United States · 2017-02-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1492-2017
Date of alert
2017-02-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Medical Systems (Cleveland) Inc
Product category
device
Product type
Devices
Reported risk: When the user performs a retrospective respiratory gated 4D CT scan with the Bellows pulmonary gating device, the CT images might be reconstructed at a single phase, while the annotations on the images incorrectly indicate that the reconstruction is from the requested specific phases (0% to 90%).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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