Consumer Products Updated 2026-10-01

Gobi Heat Rechargeable Hand Warmer Pair recalled due to fire and burn hazards

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Recalled Product

Gobi Heat Rechargeable Hand Warmer Pair


✅ What Should You Do?

  1. ⚠️ Stop using this product until you have checked the recall details below.
  2. Follow the instructions from the issuing agency (see below).
  3. 💰 Check if you are eligible for a refund or free replacement from the retailer or manufacturer.
  4. 📋 Report a product safety incident to Health Canada
Looking for a safe alternative? Search Amazon Canada for Gobi Heat Rechargeable Hand →

Hazard / Issue

Fire hazard · Burn hazard

Issued by

Consumer product safety

⚠️ What You Should Do

Consumers should immediately stop using the recalled product and contact Gobi Heat for further instructions to obtain a refund and dispose of the product.Consumers must safely dispose of the items in such a way that they cannot be used again. Contact your municipality for instructions on how to safely transport and dispose of lithium-ion batteries. Batteries are considered hazardous waste. Do not place them in household garbage.For more information, consumers can contact Gobi Heat by telephone at 1-888-462-4743, from 9:00 a.m. to 5:00 p.m. Mountain Standard Time, Monday to Friday, by email at recall@gobiheat.com or visit the company website.Joint recall with Health Canada, the United States Consumer Product Safety Commission (US CPSC) and Dragon Gear Inc. doing business as Gobi Heat.Please note the the Canada Consumer Product Safety Act prohibits recalled products from being redistributed, sold or even given away in Canada.Health Canada would like to remind consumers to report any health or safety incidents related to the use of this product or any other consumer product or cosmetic by filling out the Consumer Product Incident Report Form.This recall is also posted on the OECD Global Portal on Product Recalls website. You can visit this site for more information on other international consumer product recalls.
View official government recall