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The zipper pulls and foot grips of the George Brand Sleepers, may fall off or be removed through repeated washing, posing choking and ingestion hazards. As of September 21, 2023, the company has not received any reports of incidents or injuries in…

This recall involves one lot of cannabis extract (for inhalation) sold by Emblem Cannabis Corporation. The products were sold through authorized retailers in Ontario and Manitoba. Hazard identified The product labels have incorrect cannabinoid…

Health Canada’s sampling and evaluation program has determined that this children’s upper outwear product has a drawstring that can become caught on playground equipment, fences, or other objects and result in strangulation, or in the case of a vehicle,…

 Solution bags may be leaking in affected lots.

 Solution bags may be leaking in affected lots.

 Solution bags may be leaking in affected lots.

The recalled products do not meet the labelling and packaging requirements of the Consumer Chemicals and Containers Regulations, 2001 under the Canada Consumer Product Safety Act. The lack of appropriate labelling information could result in…

Health Canada's sampling and evaluation program has determined that the magnets do not meet the magnetic force requirements of the Toys Regulations and pose an ingestion hazard. Small, powerful magnets can be easily swallowed by children of all ages,…

 Solution bags may be leaking in affected lots.

Ortho Clinical Diagnostics (Quidelortho) determined that lots 5905-3348-1557 and 5905-3348-2899 of Vitros Lipase Slides include carts which may contain consecutive slides that may not function as intended. Quidelortho estimates that approximately 1.4% of…

Olympus is taking this recall action after discovering that the Thunderbeat's blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position. Olympus is requesting healthcare facilities…

When using this product, the footrest can loosen and fall off in some circumstances, which may result in a foot injury to user. Recall Start Date: September 15, 2023

 Affected lot may result in a false negative for skin test (pecan nut allergy)

The instructions for use (IFU) for the Atrium Ocean, Oasis, and Express chest drains do not provide sufficient precaution instruction for proper set up of catheter(s) and patient line connections with single collection chamber chest drains. Recall…

Specific lots of Cardinal Health Monoject™ luer-lock tip syringes (6 and 35 ml) have demonstrated recognition and compatibility issues with certain syringe infusion pumps. As a result, Cardinal Health recommends that they not be used with syringe…