Health product recall

Patient Tables of Philips Allura and Azurion systems

Last updated

Summary

Product
Patient Tables of Philips Allura and Azurion systems
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 catalogue number

Allura Xper FD20 (Product Of Alluraclarity Family)

Not applicable.

722028

Allura Xper FD10

Not applicable.

001443

Allura Xper FD20/20 (Product Of Alluraclarity Family)

Not applicable.

722038

Allura Xper FD10/10 (Product Of Alluraclarity Family)

Not applicable.

722027

Azurion 7 B12

Not applicable.

722 067

Allura Xper FD10 (Prouct Of Alluraclarity Family)

Not applicable.

722026

Allura Xper FD20/15

Not applicable.

722058

Azurion 7 M20

Not applicable.

722 224
722 079

Azurion 7 B20

Not applicable.

722 226
722 068

Allura Xper FD10/10 (Product Of Alluraclarity Family)

Not applicable.

722029

Azurion 7 M12

Not applicable.

722 223
722 078

Issue

Philips has identified some situations that may result in the patient falling from the table related to the mattress used on the patient table of the Philips Allura and Azurion systems: 

  • mattress slipping from the table
  • incorrect positioning of the neuro mattress on the table
  • incorrect mattress being used on the table

Recall start date: January 21, 2025

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-76910

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