Health product recall

Philips Wired Foot Switch

Last updated

Summary

Product
Philips Wired Foot Switch
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 catalogue number

Allura Xper Fd10

Not applicable.

ALLURA XPER FD10
001443

Allura Xper Fd10/10 (Product Of Alluraclarity Family)

Not applicable.

722027

Azurion7 B12

Not applicable.

722 067

Azurion7 B20

Not applicable.

722 226
722 068

Allura Xper Fd20/10 (Product Of Alluraclarity Family)

Not applicable.

722029

Allura Xper Fd20 Ortable(Product Of Alluraclarity Family)

Not applicable.

722035

Allura Xper Fd20/20 (Product Of Alluraclarity Family)

Not applicable.

722038

Multidiagnost Eleva ‐ Flat Detector ‐Image Detector

Not applicable.

0708MD02

Azurion7 M12

Not applicable.

722 223
722 078

Multidiagnost Eleva ‐ Image Intensifier‐Tv Image Detector

Not applicable.

0708MD02

Allura Xper Fd10(Product Of Alluraclarity Family)

Not applicable.

722026

Allura Xper Fd20(Product Of Alluraclarity Family)

Not applicable.

722028

Azurion7 M20

Not applicable.

722 224
722 079

Issue

Philips has become aware of a potential safety issue with the wired foot switch used with the Philips Allura Xper, Allura Centron, Azurion and Multidiagnost‐Eleva systems, where there is a possibility of loss of imaging functionality resulting from no or intermittent x‐ray radiation initiation. The wired foot switch is used to control fluoroscopy, exposure and other functions like single shot, light control, and

toggle between x‐ray planes (for bi‐plane system), this in combination with the above‐mentioned Philips systems. Evaluation of complaints received identified situations where there is a possibility for no or intermittent x‐ray radiation related to this wired foot switch. If there is no or intermittent x‐ray radiation this will lead to loss of imaging functionality which may result in delayed diagnosis or interruption of procedure.

Recall start date: August 18, 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-74216

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