RecallTracker
Canadian Recalls: Week of August 3
During the week of August 3-9, 2026, Canadian health and safety authorities issued 12 recalls: 5 from the Canadian Food Inspection Agency and 7 from Health Canada. Listeria monocytogenes contamination appeared in two separate food recalls, affecting mushrooms and cheese curds, while undeclared allergens (milk and gluten) prompted three additional product withdrawals.
CFIA — Food Safety Recalls
PC Organics and Frankie's Organic Plant-Based Cheddar baked corn puffs, Plant-Based Cheddar Jalapeno baked corn puffs, Plant-Based Cheddar baked corn crunchies, and Plant-Based Puffs Vegan Cheddar are being recalled. These products contain milk that is not declared on the label, which poses a serious health risk to consumers with milk allergies or sensitivities. Consumers should check their homes for these products, discard them, and not consume them if they have a milk allergy or sensitivity.
View full recall →Highline brand Organic Mini Bella Mushrooms Sliced is being recalled from the Canadian marketplace. The product is being recalled due to possible Listeria monocytogenes contamination. Consumers should not consume, serve, use, sell, or distribute this product and should throw it out or return it to the store where it was purchased, and contact a healthcare provider if they believe they became ill from consuming it.
View full recall →Laiterie de Coaticook Limitée is recalling multiple Mild Cheddar Curds products in white varieties, including plain, double cut, dill, spices, and hickory flavors. These products are being recalled due to possible Listeria monocytogenes contamination. Consumers should check their homes for recalled products, not consume them, and either throw them out or return them to the store where they were purchased. Anyone who believes they became ill from these products should contact their healthcare provider.
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Momchipz brand Veggie Chips (Broccoli Florets & Cauliflower) are being recalled from online distribution. The product contains undeclared gluten on the label, which poses a serious or life-threatening risk to consumers with celiac disease or other gluten-related disorders. Consumers should check their homes for the recalled product, discard it immediately, and not serve, use, sell, or distribute it.
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Kehar brand Californian Pistachio Kernel products are being recalled from the marketplace. The recall was issued due to possible Salmonella contamination in the affected products. Consumers should not consume, serve, use, sell, or distribute these recalled products and should throw them out or return them to the store where they were purchased. If you believe you became sick from consuming a recalled product, contact your healthcare provider.
View full recall →Health Canada — Consumer Products & Medical Devices
Louisville and Featherlite brand attic stairways manufactured on or before June 22, 2026, have been recalled due to defective 1/4-inch chrome-colored bolts in the spreader assembly. The bolts may not meet design specifications, creating a potential injury hazard, with 1 incident reported in Canada and 11 incidents with 1 injury reported in the United States. Consumers should immediately stop using the product and contact Louisville Ladder Corp. to receive a free repair kit containing replacement bolts, washers, and lock nuts with installation instructions.
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New Roots Herbal Inc. is recalling one lot of Probiotic Intensity in 30-count and 60-count bottles because the outer box of the 30-count bottles incorrectly claims the product contains no dairy. The product actually contains bovine colostrum, a dairy ingredient that may cause serious health risks for people with severe dairy allergies. Consumers with dairy allergies should not use this product and should consult a health care professional if they have already used it. Contact New Roots Herbal Inc. at 1-800-268-9486 or support@newrootsherbal.com with questions about the recall.
View full recall →Medtronic's Bravo CF capsule delivery system has been recalled due to an increase in complaints where the capsule fails to attach to the esophagus or detach from the delivery device. The issue stems from a potential defect in the capsule deployment component that can be worsened by failure to keep the delivery device straight as instructed, creating risks of patient aspiration, esophageal perforation, and airway obstruction. Consumers should consult the official recall notice immediately for further instructions and guidance.
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CCM Hybrid Visor and Replacement Visor accessories have been recalled, affecting 8,895 units sold in Canada. The polycarbonate portion of these visors may develop micro-fissures around the screw holes that could lead to cracking if subjected to a powerful impact such as a high-velocity puck. Consumers should immediately stop using the recalled product and contact Sport Maska Inc. (CCM) at 1-800-644-1677, Monday through Friday, 8am to 6pm ET, to receive a replacement full-face protector.
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RELLET Hyaluronic Acid Deep Hydrating Spray has been recalled in Canada, with 200 units sold. The product is missing mandatory hazard labelling required by the Cosmetic Regulations under the Food and Drugs Act, which could lead to misuse and serious injury. Consumers should immediately stop using the product and contact Joyi Supply Chain Corp at joyisupplychain@gmail.com to receive a replacement with proper labelling.
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Ultra Big Blue Automatic Toilet Bowl Cleaner has been recalled after 72,273 units were sold in Canada. The product lacks proper child-resistant packaging and does not meet required labelling standards under the Consumer Chemicals and Containers Regulations, which could result in unintentional exposure leading to serious illness or injury including death. Consumers should immediately stop using the product and dispose of it according to municipal hazardous waste guidelines, and contact Advantage Maintenance Products Ltd. at 1-800-265-9957 extension 226 for more information.
View full recall →Beckman Coulter has recalled the AU480 Immunochemistry System analyzer due to a software defect affecting units using Microsoft SQL Server 2022 Express. The defect may cause a database connection error that makes the alarmDB database unreadable, prevents the instrument from starting, and delays reporting of patient test results to physicians. Consumers should consult the official recall notice for instructions on how to address this issue.
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