Canadian Recalls: Week of May 11

Kyan Culture brand and Farm Boy brand organic microgreens have been recalled, including Organic Broccoli Microgreens, Organic Mild Mix Microgreens, Organic Spring Mix Microgreens, and Organic Microgreens in Broccoli and Mild Mix varieties. The products are being recalled due to possible contamination with pathogenic E. coli. Consumers should not consume, serve, use, sell, or distribute these products and should throw them out or return them to the store where purchased, and anyone who became sick should contact their healthcare provider.

Certain Shaoxing Cooking Wines are being recalled from the Canadian market. The product contains wheat that is not declared on the label, posing a serious health risk to consumers with wheat allergies, celiac disease, or gluten-related disorders. Consumers should check their pantries for the recalled product and not consume it if they have any wheat allergy or gluten sensitivity.

DAVIDsTEA brand Organic Sneeze Ease Herbal Infusion is being recalled in Canada. The product contains undeclared almond, a tree nut allergen, which is not listed on the label and could cause serious or life-threatening allergic reactions in sensitive consumers. Consumers should check their homes for this product, not consume it if they have a tree nut allergy or sensitivity, and throw it out or return it to the store where it was purchased.

Shirreza brand Tahini Halva with Date Sap is being recalled from the marketplace in British Columbia. The product is being recalled due to possible Salmonella contamination. Consumers should not consume, serve, use, sell, or distribute this product and should throw it out or return it to the location where it was purchased. If you believe you became sick from consuming this product, contact your healthcare provider.

Ghirardelli brand powdered beverage mixes including Premium Hot Cocoa Mix, Perfectly Premium Frappé Mix in Vanilla and Mocha varieties, and Premium Frappé Mix Frozen Hot Cocoa have been recalled. These products are being recalled due to possible Salmonella contamination. Consumers should not consume, serve, use, sell, or distribute these products, and should throw them out or return them to the location where they were purchased, and contact their healthcare provider if they believe they became sick from consuming a recalled product.

Asung Trading Inc. products have been recalled due to missing mandatory hazard labelling required by the Cosmetic Regulations under the Food and Drugs Act. The products lack proper labelling that could result in misuse and lead to serious injury to consumers. Consumers should immediately stop using the recalled products and contact Asung Trading Inc. at 416-792-2298 or info@asung.ca for a corrected label or further instructions.

Zwilling Enfinigy Electric Kettle and Zwilling Enfinigy Electric Kettle Pro models are being recalled in Canada. The kettle handles may loosen or break off during use, potentially causing hot water to spill and creating a scalding hazard to users and bystanders, including small children. Consumers should immediately stop using these products and contact Zwilling at 1-866-963-4583 or enfinigy-kettle-recall@zwilling.com to register for the return process and receive a refund.

Petzl ASTRO and CANYON GUIDE harnesses have been recalled due to a safety defect. The metal D-ring attachment pin can release and allow the attachment point to open, creating a fall hazard that could result in serious injury or death. Consumers should immediately stop using these harnesses and contact Petzl America, Inc. at 1-877-807-3805 (8:00 a.m. to 4:00 p.m. MT, Monday through Friday) to obtain a free replacement kit with installation instructions.

Petzl has recalled certain SIMBA and SWAN harnesses due to a defect in the FAST LT PIN-LOCK buckle. A missing rivet in the buckle could cause it to open unexpectedly, creating a fall hazard that could result in serious injury or death. Consumers should immediately stop using the recalled harnesses and contact Petzl America, Inc. at 1-877-807-3805 for a free replacement.

The Endoflip System, including EF and ES catheters used with EF-100 systems, has been recalled due to a performance defect. After January 1, 2026, the system will incorrectly mark catheters as expired due to a 24-hour usage limit, making them unavailable for clinical procedures. Consumers should consult the official recall notice for further information and guidance.

Medtronic has recalled the Octopus Nuvo, Octopus Evo AS, and Octopus 4 canister tubing sets due to a manufacturing defect identified on January 7, 2026. The short tube was incorrectly attached to the bottom of the canister and the long tube to the top, which is the reverse of the proper design specification. Consumers should check the official recall notice for instructions on how to proceed.

Abiomed, Inc. has issued a voluntary recall of the Automated Impella Controller (AIC) used with left ventricular Impella devices. A potential software error may cause the device to unexpectedly restart in specific clinical circumstances, which could lead to serious injury or death in certain patients. Consumers should review the official recall notice for detailed information and guidance from healthcare providers.