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

Recall Z-0832-2014 — Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems, Philips Healthcare, Cleveland, OH The Brilliance iCT and iCT SP are whole body Computed Tomography X-Ray Systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data take

U.S. FDA — Device Enforcement · United States · 2013-12-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0832-2014
Date of alert: 2013-12-09
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: Patient images exhibited ring artifacts.

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

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