Health product recall

Philips Allura Xper

Last updated

Summary

Product
Philips Allura Xper
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

Allura Xper FD20 OR Table (Product Of Alluraclarity Family)

Not applicable.

722035

Allura Xper FD10/10 (Product Of Alluraclarity Family)

Not applicable.

722027

Allura Xper FD20/10 (Product Of Alluraclarity Family)

Not applicable.

722029

Allura Xper FD10

Not applicable.

001443

Allura Xper FD20 (Product Of Alluraclarity Family)

Not applicable.

722028

Issue

Philips has identified potential safety issues with delayed LTE kit installations for Allura R7.6-R8.1 systems exceeding 10 years of life. The kit includes a propeller motor clamping bolt and the x-ray tube locking bolt. If one of these bolts breaks, part of the system will not function as expected.

Recall Start Date: November 18, 2024

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies

Philips Medical Systems Nederland B.V.

Veenpluis 6, Best, Netherlands, 5684 PC

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-76616

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