Brand Recall Hub

Lse Recalls in Canada

49 recalls found for Lse. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

49 Lse Recalls

Medical Devices Type II
2026-03-13

SOLTIVE Premium SuperPulsed Laser System

Performance

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Medical Devices Type II
2026-01-29

ShockPulse-Se Lithotripsy System and ShockPulse Lithotripsy Generator

Performance

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Medical Devices Type II
2025-12-31

ShockPulse Lithotripsy System, Generator and Transducer

Performance

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Medical Devices Type II
2025-10-28

Schiller EASY PULSE®

Performance

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Medical Devices Type II
2025-10-24

ShockPulse Lithotripsy Transducer

Performance

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Medical Devices Type II
2025-10-15

Eterna™ Implantable Pulse Generator

Device compatibility - Performance

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Consumer Products
2025-07-31

DT Swiss carbon fiber wheelsets recalled due to fall hazard

Fall hazard

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Medical Devices Type II
2025-07-18

Vercise Genus™ R 16 and R32 Implantable Pulse Generator Kits

Performance

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Medical Devices Type I
2025-03-24

Autopulse Nxt Resuscitation System

Performance

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Medical Devices Type I
2025-02-25

VARIPULSE™ Bi-Directional Ablation Catheter

Labelling and packaging

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Medical Devices Type II
2024-09-25

SOLTIVE™ Premium SuperPulsed Laser System

Performance

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Medical Devices Type II
2024-08-14

Wavewriter Alpha Implantable Pulse Generator Kit

Performance

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Medical Devices Type I
2024-08-12

Vercise Genus ™ R16 and R32 Implantable Pulse Generator (IPG) Kits

Performance

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Medical Devices Type II
2024-07-04

Proclaim Implantable Pulse Generators

Labelling and packaging - Performance

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Medical Devices Type II
2024-07-03

Infinity 5 and 7 Implantable Pulse Generator

Labelling and packaging - Performance

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Medical Devices Type I
2024-03-28

Rad-G Pulse Oximeters

Performance

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Medical Devices Type II
2024-02-29

SOLTIVE™ Premium SuperPulsed TF Laser System

Performance

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Medical Devices Type II
2024-01-05

Pulse*Spray® Infusion Systems 3fx135x120

Performance

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Medical Devices Type II
2024-01-04

SOLTIVE™ SuperPulsed Laser Ball Tip Fiber Single Use

Sterility

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Medical Devices Type II
2023-12-15

Soltive Superpulsed Laser Fiber Single Use

Labelling and packaging

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Medical Devices Type II
2023-10-17

Emblem S-ICD Pulse Generator and Emblem MRI S-ICD Pulse Generator

Performance

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Health Products Type I
2023-09-29

Allergenic Extract Non Pollens (Pecan Nut): False negative for skin test

Product quality

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Health Products Type I
2023-09-07

Allergenic Extract Non Pollens: False negative for skin test

Product quality

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Medical Devices Type II
2023-08-15

Proclaim and Infinity Implantable Pulse Generators

Performance

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Medical Devices Type II
2023-06-14

Flexiva™ Pulse Tractip™

Performance

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Health Products Type I
2022-12-14

Allergenic extract non pollens (Peanut allergy): False negative for skin test

Product quality

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Consumer Products
2022-11-16

Various Goalsetter Wall-Mounted Basketball Goals recalled due to impact injury hazard and risk of death to consumers

Injury hazard

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Health Products Type I
2022-11-15

Allergenic extract non pollens (Peanut allergy): False negative for skin test

Product quality

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Medical Devices Type I
2022-08-02

Assurity Mri Pulse Generator

Performance

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Medical Devices Type II
2022-06-27

Fingertip Pulse Oximeter

Unauthorised device

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Showing 30 of 49 recalls. View all →