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

Recall Z-0335-2014 — Brilliance iCT Computed Tomography X-Ray System, Product Usage: The Brilliance iCT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.

U.S. FDA — Device Enforcement · United States · 2013-10-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0335-2014
Date of alert
2013-10-11
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: If the couch, with the footrest extension attached, is positioned where the table travel is within the bore of the gantry, and the user begins to lower the couch, the footrest extension can contact the gantry cover or come in contact with the user due to the length of the accessory.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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