Brand Recall Hub

Bod Recalls in Canada

34 recalls found for Bod. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

34 Bod Recalls

Consumer Products
2026-04-10

TJ Trading Co. Inc. products recalled due to missing mandatory hazard labelling

Labelling and packaging

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Consumer Products
2026-01-21

Truly Tallow All-in-1 Mens Face + Body + Hair Whipped Tallow recalled due to a chemical hazard

Chemical hazard

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Medical Devices Type II
2025-10-14

Catalyft™ PL Expandable Interbody System, Interbody Cage

Performance

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Medical Devices Type II
2025-01-29

Clarity II Main System Body

Performance

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Consumer Products
2024-08-22

3-Colour Face and Body Paint recalled due to chemical hazard

Chemical hazard

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Medical Devices Type I
2024-03-06

BD Bodyguard Microset

Performance

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Food Class 2
2023-08-24

BodyArmor brand drinks recalled due to over-fortification of vitamins and minerals and labelling issues

Chemical

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Medical Devices Type II
2023-06-01

Ogival Interbody Cage, PEEK

Labelling and packaging

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Medical Devices Type II
2023-03-15

BD Bodyguard Microset

Performance

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Consumer Products
2022-10-28

Body Glove Tandem Inflatable 2-Person Paddleboard recalled due to potential drowning hazard

Drowning hazard

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Medical Devices Type II
2022-09-20

Anti-GM1 Autoantibodies Elisa IVD Test

Performance

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Health Products Type I
2022-06-21

Produits de Bien-Être Bodispa recalls sexual enhancement products due to the potential presence of undeclared prescription drug ingredients.

Undeclared substance

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Medical Devices Type II
2021-10-08

Bodyguard pumps (2021-09-16)

Medical devices

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Medical Devices Type II
2020-10-09

CME America BodyGuard Infusion Administration Sets (2020-06-16)

Medical devices

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Medical Devices Type III
2020-06-05

Body Fluid Controls (2020-05-18)

Medical devices

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Medical Devices Type I
2020-06-02

CME BodyGuard Infusion Pump System (2020-03-06)

Medical devices

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Medical Devices Type II
2020-04-15

Bodyguard Microset (2020-01-14)

Medical devices

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Medical Devices Type III
2020-01-10

CMF Distraction System - Mandible Cloverleaf Foot, AB & BC Craniofacial Distractor Body (2019-11-28)

Medical devices

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Medical Devices Type III
2019-12-03

Kappa (EP171) Rabbit Monoclonal Primary Antibody - Predilute (2019-07-30)

Medical devices

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Medical Devices Type III
2019-11-29

ID- Fungal Antibody System - Histoplasma (2019-11-06)

Medical devices

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Medical Devices Type II
2019-11-01

BodyGuard Microset (2019-10-03)

Medical devices

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Consumer Products
2019-07-17

Bodum Bistro Two-Slice and Four-Slice Toasters recalled due to shock hazard

Electrical hazard

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Consumer Products
2019-05-27

Bodum CHAMBORD® Stove Top Espresso Maker recalled due to Fire and Burn Hazards

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Medical Devices Type II
2019-05-17

UniCel DxI 600, 800 Access Immunoassay Systems (Thyroglobulin Antibody II, Free T3 Assay, Free T4 Assay, Total T3 Assay, Thyroglobulin Assay, GI Monitor (CA 19-9))(2019-04-22)

Medical devices

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Consumer Products
2019-05-01

Bodum + Starbucks Recycled Coffee Press recalled due to a laceration risk

Laceration hazard

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Medical Devices Type II
2019-04-29

BOD POD, PEA POD Body Composition Tracking Systems (2019-04-17)

Medical devices

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Medical Devices Type III
2019-03-15

Factor XIIIa Antibody (2018-09-30)

Medical devices

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Medical Devices Type III
2019-03-08

UniCel DxI 600, 800 Access Immunoassay System - Thyroglobulin Antibody II (2019-02-09)

Medical devices

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Other
2018-11-22

Foreign Product Alert: Black Lion Pill, Help 100% & Pure Natural & Body Slim capsules, Herba Saraf, Horny Little Devil, Ja Dera Max+ capsules, Lida (Plus) capsules, Nutra Organics Green Tea Extract capsules, Papapa, Red Zone Xtreme 3000, Rhino 69 Ext...

Undeclared substance

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Medical Devices Type II
2018-09-17

Various Roche Detection, Amplification Kits and Primary Antibody (2018-08-16)

Medical devices

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Showing 30 of 34 recalls. View all →