Health product recall

Philips Allura Xper and Azurion 7 Systems

Last updated

Summary

Product
Philips Allura Xper and Azurion 7 Systems
Issue
Medical devices - Performance issue
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 (Product Of Alluraclarity Family)

Not applicable.

722026

Azurion 7 M20

Not applicable.

722 224
722 079

Allura Xper FD20/20 (Product Of Alluraclarity Family)

Not applicable.

722038

Allura Xper FD20/15

Not applicable.

722058

Allura Xper FD20 (Product Of Alluraclarity Family)

Not applicable.

722028

Azurion 7 M12

Not applicable.

722 078

Allura Xper FD10

Not applicable.

001443

Issue

Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are:

• Loss of bluetooth connection due to interferences from other radio equipment

• Battery not fully charged

• Battery not holding its charge

• Damage in the charger, cable and/or connector of the wireless foot switch

Recall start date: July 4, 2023

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-73951

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe