Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
Reported: February 17, 2016 Initiated: November 3, 2015 #Z-0764-2016
Product Description
Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
Reason for Recall
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).
Details
- Recalling Firm
- Philips Electronics North America Corporation
- Units Affected
- 15 subject to correction and removal
- Distribution
- Worldwide Distribution. US states of TN and IN and the countries of Australia, Belgium, Egypt, France, Germany, Japan, Republic of Korea, Netherlands, and Saudi Arabia.
- Location
- Andover, MA
Frequently Asked Questions
What product was recalled? ▼
Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.. Recalled by Philips Electronics North America Corporation. Units affected: 15 subject to correction and removal.
Why was this product recalled? ▼
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).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 17, 2016. Severity: Moderate. Recall number: Z-0764-2016.
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