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

Recall Z-0764-2016 — Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.

U.S. FDA — Device Enforcement · United States · 2015-11-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0764-2016
Date of alert
2015-11-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Electronics North America Corporation
Product category
device
Product type
Devices
Reported risk: Normally, movement of the C-arc is initially stopped by the motor (holding torque) then by the electromagnetic brake, leading to a full stop of the C-arc. Because of improper adjustment and tolerances, when the C-arc is initially stopped in an unbalanced position, the air gap of the brake can become too large, resulting in continued C-arc movement (C-arc is looking for balanced position).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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