Brand Recall Hub

K Act Recalls in Canada

371 recalls found for K Act. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

371 K Act Recalls

Health Products Type III
2026-04-01

Health First Vitamin E capsule; Undeclared active ingredient

Product quality

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Consumer Products
2026-03-20

Vevor Retractable Baby Gates recalled due to entrapment hazard

Entrapment hazard

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Medical Devices Type II
2026-03-17

RAPIDPoint® 500 Blood Gas Systems

Performance

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Other
2026-03-11

Nextleaf Labs Ltd. recalls Glacial Gold – Anytime 1:1 Fuzzy Mango due to packaging and labelling issue

Labelling and packaging

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Other
2026-03-09

IXCHIQ (chikungunya vaccine, live, attenuated) and the Risk of Serious Adverse Reactions in Medically Frail Individuals 65 Years of Age and Older

New safety information - Product safety - Adverse reaction

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Consumer Products
2026-02-26

Tubby Tots Fizzy Flash Bath Magic recalled due to injury and impact hazard

Injury hazard - Impact hazard

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Consumer Products
2026-02-20

Custom-made window coverings manufactured by Apara-Transiplast recalled due to choking hazard for children

Choking hazard

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Health Products Type II
2026-02-16

APO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution

Product quality

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Health Products Type II
2026-02-09

TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution

Product quality

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Consumer Products
2026-01-22

Angry Orange Stain Removers recalled due to risk of exposure to bacteria

Microbial hazard

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Health Products Type I
2026-01-13

Octreotide for injectable suspension; Good manufacturing practices concerns

Product quality

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Consumer Products
2025-12-04

Grizzly G0815 15-inch 3 HP Heavy-Duty Planer recalled due to impact and laceration hazards

Impact hazard - Laceration hazard

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Consumer Products
2025-11-19

Health Canada warns that Gniby Rechargeable Green Powerful Tactical Flashlight with Adjustable Focus, Green Laser Pointer, previously available on Amazon.ca, may pose a risk of permanent eye injury

Injury hazard

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Medical Devices Type II
2025-11-14

BD BACTEC™ MGIT™ 960 PZA Kit

Labelling and packaging

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Food
2025-11-14

ByHeart Whole Nutrition Infant Formula may be unsafe due to potential presence of dangerous bacteria Clostridium botulinum

Clostridium botulinum

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Consumer Products
2025-11-13

MÖBI Zippee Activity Toy recalled due to choking hazard

Choking hazard

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Consumer Products
2025-11-13

Q’Straint QRT-DELUXE and Q’Straint QRT-MAX retractors recalled due to injury hazard

Injury hazard

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Medical Devices Type II
2025-11-13

Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette

Labelling and packaging

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Medical Devices Type II
2025-11-13

Access 2 Reaction Vessels

Performance

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Health Products Type II
2025-11-05

Proactiv / Proactiv + BPO Products: Benzene Concentration Outside Allowable Limit

Product safety

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Other
2025-10-28

Culture Kizos inc./Kizos Culture inc. recalls Coterie - Prickly Pear Liquid Diamonds - 1g due to labelling issue

Labelling and packaging

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Consumer Products
2025-10-10

Health Canada warns that Gniby LED Pointer, 3 in 1 rechargeable interactive laser toy for cats and dogs previously available on Amazon.ca may pose a risk of permanent eye injury

Injury hazard

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Other
2025-10-10

Culture Kizos inc./Kizos Culture inc. recalls Coterie Double-Infused Fruity Pebbles Blunt due to microbial contamination

Microbial contamination

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Vehicles
2025-10-08

Transport Canada Recall - 2025505 - AMERICAN MANUFACTURING OPERATIONS

Structure

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Medical Devices Type II
2025-10-07

Precision1 One-Day Contact Lenses

Labelling and packaging - Sterility

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Other
2025-10-02

Sensi Brands Ltd. recalls Wintermint Chillows and Cinnamon Chillows due to product quality issue

Suspected quality concern - Labelling and packaging

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Health Products Type III
2025-09-25

No7 Restore & Renew Face & Neck Multi Action Day Cream SPF 30; No QA authorization

Other

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Medical Devices Type II
2025-09-17

TactiFlex™ Ablation Catheter, Sensor Enabled™

Labelling and packaging - Performance

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Health Products Type III
2025-09-08

Sunforce Health & Organics products recall; Deficiencies in Good Manufacturing Practices

Product quality

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Health Products Type III
2025-09-08

NazalActin Liquid: No market authorization, incorrect NPN, deficiencies in Good Manufacturing Practices

Product quality

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Showing 30 of 371 recalls. View all →