Brand Recall Hub

Xper Recalls in Canada

32 recalls found for Xper. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

32 Xper Recalls

Medical Devices Type II
2026-03-17

Allura Xper and Azurion Systems

Performance

View recall details →
Medical Devices Type II
2026-01-06

Allura Xper and Allura CV20 Systems

Performance

View recall details →
Medical Devices Type II
2025-11-19

Xpert® BCR-ABL Ultra

Performance

View recall details →
Medical Devices Type II
2025-10-24

Xpert® CT/NG

Performance

View recall details →
Consumer Products
2025-09-24

Clementoni Super Chemistry Lab science experiment kits recalled due to missing bilingual hazard labelling

Chemical hazard

View recall details →
Medical Devices Type II
2025-09-24

Allura Xper Systems

Performance

View recall details →
Medical Devices Type II
2025-09-24

Allura Xper Systems

Performance

View recall details →
Medical Devices Type II
2025-08-15

Allura Xper Systems

Device compatibility

View recall details →
Medical Devices Type II
2024-11-29

Philips Allura Xper

Performance

View recall details →
Medical Devices Type II
2024-09-09

Philips Azurion, Allura Xper and Eleva Systems

Performance

View recall details →
Medical Devices Type I
2024-01-19

Philips Allura XPER, Allura Centron and Azurion Systems

Performance

View recall details →
Medical Devices Type II
2023-08-21

Philips Multidiagnost Eleva, Allura Xper and Azurion systems

Performance

View recall details →
Medical Devices Type II
2023-07-13

Philips Allura Xper and Azurion 7 Systems

Performance

View recall details →
Medical Devices Type II
2023-02-22

Tracoe Experc Sets

Labelling and packaging

View recall details →
Medical Devices Type II
2022-12-01

Tracoe Experc Percut Dilation Sets

Performance

View recall details →
Medical Devices Type II
2022-09-20

Xpert EV Assay

Performance

View recall details →
Medical Devices Type II
2021-12-13

Allura Xper Fd10 & Fd20 products

Mechanical defect

View recall details →
Medical Devices Type II
2021-11-25

ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)

Software defect

View recall details →
Medical Devices Type II
2021-11-12

ALLURA XPER and AZURION 7

Software defect

View recall details →
Medical Devices Type II
2021-04-14

XPER FLEX CARDIO PHYSIOMONITORING SYSTEM (2021-04-01)

Medical devices

View recall details →
Other
2020-06-22

Get ready for this summer’s heat with expert tips!

Product safety

View recall details →
Medical Devices Type II
2019-11-01

Xpert Xpress Flu/RSV (2019-10-07)

Medical devices

View recall details →
Medical Devices Type II
2019-03-08

MultiDiagnost Eleva - Image Intensifier and Flat Detector, ALLURA XPER (FD10, FD20, FD20/10, FD20/15, FD20/20) (2019-02-24)

Medical devices

View recall details →
Medical Devices Type III
2019-02-22

Cepheid Xpert Respiratory Control Panel (2019-01-30)

Medical devices

View recall details →
Medical Devices Type II
2018-11-30

Xper Flex Cardio Physiomonitoring System-Main Unit (2018-11-18)

Medical devices

View recall details →
Medical Devices Type II
2018-08-17

Allura Xper FD10, FD20, FD10/10, and FD20/10 (2018-06-12)

Medical devices

View recall details →
Medical Devices Type II
2018-08-02

Allura Xper FD10/10 - Main Unit, Allura Xper FD10, Allura Xper FD20 - Main Unit and Allura Xper FD20/10 System - Main Unit (2018-07-17)

Medical devices

View recall details →
Medical Devices Type II
2018-04-24

Allura XPER Systems (2018-03-19)

Medical devices

View recall details →
Medical Devices Type II
2018-04-13

Xper Flex Cardio Physiomonitoring System-Main Unit (2018-03-13)

Medical devices

View recall details →
Medical Devices Type II
2018-02-01

Xpert GBS Assay (2017-12-08)

Medical devices

View recall details →

Showing 30 of 32 recalls. View all →