Philips Allura Xper FD20 Ceiling version only recall
Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
Why was Philips Allura Xper FD20 Ceiling version only 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).
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Ceiling version only.
- Product
- Philips Allura Xper FD20 Ceiling version only; 722028; imaging applications.
- Recalling firm
- Philips Electronics North America Corporation
- Quantity
- 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.
- Recall date
- February 17, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)