Public recall detail

Philips Allura Xper and Azurion 7 Systems

2023-07-13

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Recall Safety notice
Quick summary

Quick summary: Philips Allura Xper and Azurion 7 Systems. Date: 2023-07-13.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Philips Allura Xper and Azurion 7 Systems. Date: 2023-07-13.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
ProductPhilips Allura Xper and Azurion 7 Systems
IssueMedical devices - Performance
Recall classType II
IdentificationRA-73951

Affected products

ProductAllura Xper FD20 Or Table (Product Of Alluraclarity Family)
LotNot applicable.
Model722035
Serial numberNot applicable.
DescriptionAllura Xper FD20 Or Table (Product Of Alluraclarity Family)
ProductAllura Xper FD10 (Product Of Alluraclarity Family)
LotNot applicable.
Model722026
Serial numberNot applicable.
DescriptionAllura Xper FD10 (Product Of Alluraclarity Family)
ProductAzurion 7 M20
LotNot applicable.
Model722 224 722 079
Serial numberNot applicable.
DescriptionAzurion 7 M20
ProductAllura Xper FD20/20 (Product Of Alluraclarity Family)
LotNot applicable.
Model722038
Serial numberNot applicable.
DescriptionAllura Xper FD20/20 (Product Of Alluraclarity Family)
ProductAllura Xper FD20/15
LotNot applicable.
Model722058
Serial numberNot applicable.
DescriptionAllura Xper FD20/15
ProductAllura Xper FD20 (Product Of Alluraclarity Family)
LotNot applicable.
Model722028
Serial numberNot applicable.
DescriptionAllura Xper FD20 (Product Of Alluraclarity Family)
ProductAzurion 7 M12
LotNot applicable.
Model722 078
Serial numberNot applicable.
DescriptionAzurion 7 M12
ProductAllura Xper FD10
LotNot applicable.
Model001443
Serial numberNot applicable.
DescriptionAllura Xper FD10

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

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Radiology
CompaniesPhilips Medical Systems Nederland B.V. Veenpluis 6, Best, Netherlands, 5684 PC
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-73951
Background{}
CompaniesPhilips Medical Systems Nederland B.V. Veenpluis 6, Best, Netherlands, 5684 PC
AudiencesHealthcare
Source updated2023-07-13

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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