Brand Recall Hub

Azurion Recalls in Canada

31 recalls found for Azurion. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

31 Azurion Recalls

Medical Devices Type II
2026-03-17

Allura Xper and Azurion Systems

Performance

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Medical Devices Type II
2025-12-29

Azurion R2.1.10 and R2.2.10 systems

Performance

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Medical Devices Type II
2025-12-18

Azurion R3.0 Systems

Performance

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Medical Devices Type II
2025-08-15

Allura and Azurion Systems

Performance

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Medical Devices Type II
2025-06-19

Azurion 7 M20

Performance

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Medical Devices Type II
2025-06-12

Azurion 7 Systems

Performance

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Medical Devices Type II
2025-02-06

Patient Tables of Philips Allura and Azurion systems

Performance

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Medical Devices Type II
2025-01-30

Azurion and Allura Systems

Performance

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Medical Devices Type II
2024-12-30

Azurion and Allura Systems

Performance

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Medical Devices Type II
2024-09-09

Philips Azurion, Allura Xper and Eleva Systems

Performance

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Medical Devices Type II
2024-08-26

Azurion 7 M20

Performance

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Medical Devices Type II
2024-08-14

Azurion 3 and 7

Performance

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Medical Devices Type I
2024-01-19

Philips Allura XPER, Allura Centron and Azurion Systems

Performance

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Medical Devices Type II
2024-01-05

Azurion 7 System

Performance

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Medical Devices Type II
2024-01-04

Azurion 7 M20

Performance

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Medical Devices Type II
2024-01-04

Azurion 7 M20

Performance

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Medical Devices Type II
2023-11-24

Philips Allura and Azurion

Performance

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Medical Devices Type II
2023-08-21

Philips Multidiagnost Eleva, Allura Xper and Azurion systems

Performance

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Medical Devices Type II
2023-07-13

Philips Allura Xper and Azurion 7 Systems

Performance

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Medical Devices Type II
2023-06-22

Philips Azurion and Allura Systems

Performance

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Medical Devices Type II
2023-03-31

Philips Azurion System

Performance

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Medical Devices Type II
2021-11-12

ALLURA XPER and AZURION 7

Software defect

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Medical Devices Type II
2021-10-15

AZURION products (2021-09-27)

Medical devices

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Medical Devices Type II
2020-05-01

AZURION 7 M20 (2020-04-09)

Medical devices

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Medical Devices Type III
2020-05-01

AZURION 7 M20 (2020-04-03)

Medical devices

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Medical Devices Type II
2020-04-15

Azurion 7 M20 (2020-03-03)

Medical devices

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Medical Devices Type II
2020-01-06

AZURION 7 M20, B12 and B20 (2019-12-18)

Medical devices

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Medical Devices Type II
2019-11-15

Azurion 7M12, M20, B12 & B20 (2019-11-04)

Medical devices

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Medical Devices Type II
2019-07-19

Azurion 7 M12, M20 (2019-07-05)

Medical devices

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Medical Devices Type II
2019-07-19

Azurion 7 M12, M20 (2019-07-05)

Medical devices

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Showing 30 of 31 recalls. View all →