Canada Recalls Siberia and ZYN Nicotine Pouches Over Unauthorized Sales

Jun.15
Canada Recalls Siberia and ZYN Nicotine Pouches Over Unauthorized Sales
Health Canada has issued a nationwide recall for nicotine pouch products sold under the Siberia and ZYN brands, citing a lack of market authorization. All affected lots are subject to the recall.

Key Points

  • Nationwide recall issued;
  • Siberia and ZYN affected;
  • Unauthorized sales cited;
  • All lots impacted;
  • Classified as Type II recall.

2Firsts

June 15, 2026

Health Canada has issued a nationwide recall affecting nicotine pouch products sold under the Siberia and ZYN brands, citing unauthorized sales in the Canadian market.

According to the recall notice, the affected Siberia products are 35 mg nicotine pouches in Super Slim, White Dry, Power White and White Slim varieties. All lots are included in the recall.

The recall also covers ZYN 6 mg nicotine pouch products in Cool Mint, Wintergreen, Spearmint, Menthol, Chill and Peppermint varieties, with all lots affected.

Brand

Nicotine Strength

Affected Flavours / Types

Lots Affected

Reason for Recall & Potential Risks

ZYN

6 mg

Cool Mint, Wintergreen, 

Spearmint, Menthol, Chill, Peppermint

All lots

Reason: Sold without market authorization (Drug Identification Number - DIN) from Health Canada.

Risks: Categorized as a Type II recall (the probability of serious adverse health consequences is remote). 

However, without regulatory oversight, there is no guarantee regarding ingredients, safety, or labeling compliance.

Siberia

35 mg

(Extremely High)

Super slim, white dry, power white, white slim

All lots

Reason: Sold without market authorization (DIN) in Canada.

Risks: 35 mg represents an extremely high nicotine concentration

Unauthorized high-dose nicotine products pose severe risks of acute poisoning, 

leading to symptoms like rapid heart rate, severe nausea, dizziness, or respiratory issues.

Health Canada said the recall was not triggered by a product-quality defect but because the products were being sold without market authorization in Canada.

The agency classified the action as a Type II recall. Under Health Canada’s classification system, a Type II recall involves products whose use or exposure may cause temporary adverse health consequences, while the probability of serious adverse health effects is considered remote.

Consumers are advised to verify whether they possess affected products.

For individuals currently using the products, Health Canada recommends consulting a healthcare provider before discontinuing use, particularly for regular users or those with nicotine dependence.

Consumers with questions are encouraged to contact the recalling company directly.

The agency also called on consumers to report adverse reactions, health incidents and product safety concerns associated with the recalled products.

The recall is notable because ZYN has become one of the fastest-growing modern oral nicotine brands globally. Its parent company, Philip Morris International (PMI), has continued expanding the product’s presence across the United States and other international markets.

Canada currently permits the sale of nicotine pouch products only if they have received appropriate regulatory authorization. Since 2024, the federal government has tightened controls on nicotine pouches, requiring approved products to be sold primarily through pharmacies while introducing stricter labeling, advertising and flavor restrictions.

Industry observers say the recall underscores continued regulatory scrutiny of unauthorized nicotine products in Canada and highlights how governments are strengthening market-access and compliance requirements as the nicotine pouch category expands globally.

Cover image: 604 Now


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