Philips Healthcare IQon Spectral CT computed tomography recall
Philips Healthcare IQon Spectral CT computed tomography x-ray system
Why was Philips Healthcare IQon Spectral CT computed tomography recalled?
There is a possibility that screws holding an internal portion of the gantry (Reaction Ring) to the scanner s main bearing may come loose. If this occurs, the part(s) will not be expelled, however, a noise may be heard coming from the gantry.
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?
IQon Spectral CT 728332 Devices manufactured 03/05/2009 to present.
- Product
- Philips Healthcare IQon Spectral CT computed tomography x-ray system
- Recalling firm
- Philips Medical Systems (Cleveland) Inc
- Quantity
- 50
- Distribution
- 107 domestic accounts 15 US Govt accounts 682 Foreign Accounts 3 Mexico accounts 12 Canada accounts
- Recall date
- January 17, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)