Brand Recall Hub

Pat Recalls in Canada

99 recalls found for Pat. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

99 Pat Recalls

Medical Devices Type II
2026-04-14

Mixing Bowl And Spatula, 20- Pack

Sterility

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Medical Devices Type II
2025-01-30

Philips Breast Coils

Performance

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Medical Devices Type II
2026-02-20

Philips IntelliVue Patient Monitors

Performance

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Consumer Products
2026-02-17

Patchwork and Pine Inc. Lip Balm and Artisan Soap recalled due to the presence of prohibited ingredients

Chemical hazard

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Medical Devices Type II
2025-12-31

Patient Information Center IX

Device compatibility

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Medical Devices Type II
2025-12-23

Edan Patient Monitors

Labelling and packaging

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Medical Devices Type II
2025-09-24

BD Alaris™ Pump Module and subset of Compatible Pump Infusion Sets

Performance

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Medical Devices Type I
2025-08-28

BeneVision N1 Patient Monitor

Performance

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Other
2025-08-25

Important Safety Information on CRYSVITA (burosumab) and the Risk of Severe Hypercalcemia in Patients with Tertiary Hyperparathyroidism

New safety information - Product safety

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Medical Devices Type I
2025-06-25

Nellcor™ Bedside SpO2 Patient Monitoring System

Performance

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Food Class 1
2025-06-04

North Shore Fishery brand Frozen Breaded Shrimp Patties and Frozen Tempura Shrimp Roll recalled due to undeclared egg, soy and milk

Egg - Soy - Milk

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Food Class 1
2025-05-10

Fruit Dôme brand Thyme recalled due to pathogenic E.coli

E. Coli - other pathogenic

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Medical Devices Type I
2025-05-02

Endopath Echelon Vascular Reloads

Performance

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Food Class 1
2025-02-22

Jean Perrin brand Morbier de Scey and Raclette de Scey (cheeses) recalled due to possible contamination with pathogenic E. coli

E. Coli - other pathogenic

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Medical Devices Type II
2025-02-06

Patient Tables of Philips Allura and Azurion systems

Performance

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Food Class 1
2025-01-31

Jean Perrin brand Morbier (cheese) recalled due to pathogenic E.coli

E. Coli - other pathogenic

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Food Class 1
2025-01-18

Sweet Cream brand Mini Patisserie recalled due to Salmonella

Salmonella

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Medical Devices Type II
2024-12-12

Medline Industries Kits containing Non-Sterile Codman Surgical Patties and Strips produced by Integra Lifesciences

Sterility

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Health Products Type II
2024-12-06

Absorbine Jr. Extra Strength Multi Use Patch: Voluntary recall due to significant violations to the GMPs

Product quality

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Medical Devices Type II
2024-11-21

Presource® kits containing Codman® Patties & Strips© components produced by Integra Lifesciences

Sterility

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Medical Devices Type II
2024-11-21

Presource® kits containing Codman® Patties & Strips© components produced by Integra Lifesciences

Sterility

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Medical Devices Type II
2024-10-24

CODMAN® Surgical Strips and Patties X-Ray Detectable

Sterility

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Medical Devices Type II
2024-10-18

CardioMEMS Patient Electronics System

Performance

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Medical Devices Type II
2024-09-18

IntelliVue MX550 Patient Monitor

Performance

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Other
2024-07-31

Mega 2000™ and Mega Soft™ Patient Return Electrodes - Potential Risk of Patient Burn Injuries

Revised instructions for use - Labelling and packaging - Increased risk or new adverse events

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Medical Devices Type II
2024-07-02

Volara System Single Patient Use Circuit

Performance

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Medical Devices Type I
2024-06-26

Mega2000 Patient Return Electrode

Performance

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Medical Devices Type II
2024-06-07

Zoll ventilators with MRI compatibility

Labelling and packaging

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Medical Devices Type II
2024-06-05

Deep Brain Stimulation Clinician and Patient Programmer Applications

Performance

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Medical Devices Type I
2024-05-15

Mega Soft Universal Patient Return Electrode

Performance

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Showing 30 of 99 recalls. View all →