Vicks inhaler recall overview:
- Who: Kaz USA Inc., a Helen of Troy company, is recalling all lots of the Vicks Sinus Steam Inhaler (VIH200CV1).
- Why: The product was distributed in Canada without the required Medical Device License (MDL).
- Where: The recall is effective in Canada.
Kaz USA Inc., a Helen of Troy company, is recalling the Vicks Sinus Steam Inhaler (model VIH200CV1).
This recall affects all lots of the product, which is categorized under medical devices for ear, nose, and throat use.
The Vicks recall, officially announced on Feb. 3, was later updated on Feb. 25. According to Health Canada, the Vicks Sinus Steam Inhaler was distributed without the required authorization under the Health Canada medical devices regulations.
“The Vicks Sinus Steam Inhaler was distributed in Canada without the required Medical Device License (MDL) under the Health Canada medical devices regulations,” the Vicks recall says.
Consumers advised to discontinue use of unauthorized inhaler
The recall notice advises consumers to stop using the Vicks Sinus Steam Inhaler immediately due to its unauthorized status in Canada.
Kaz USA is taking steps to address the issue by recalling all affected units of the Vicks Sinus Steam Inhaler from the Canadian market. The company is working closely with Health Canada to ensure that all regulatory requirements are met and that the product is removed from distribution channels.
For more information about the Vicks recall, consumers can contact Kaz USA at 1-800-827-6712.
Further details and updates on the recall can also be found on the Health Canada website.
Kaz USA says it has not received any reports of illness or injury related to the recall so far. The company is not currently facing legal action over the Vicks recall, but Top Class Actions follows recalls closely as they sometimes lead to class action lawsuits.
Are you affected by this Vicks Sinus Steam Inhaler recall? Let us know in the comments.
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