Quick summary: TUMS Peppermint Regular Strength tablets: One lot recalled due to contamination. Date: 2022-11-30.
TUMS Peppermint Regular Strength tablets: One lot recalled due to contamination
2022-11-30
Recommended action: stop using or consuming the product if you believe it matches the recall, review the official details, and follow the instructions from the official source.
Recall details
Quick summary: TUMS Peppermint Regular Strength tablets: One lot recalled due to contamination. Date: 2022-11-30.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
Issue
GlaxoSmithKline Consumer Healthcare ULC is recalling one lot of TUMS Peppermint Regular Strength tablets after some tablets were found to contain fragments of fibreglass and other material, including paper and aluminum foil. The product is sold in a package of three rolls containing 12 tablets each, and was distributed across Canada starting on October 25, 2022. TUMS is an antacid indicated for adult use to relieve indigestion and heartburn caused by too much acid in the stomach. If consumed, the fragments should pass through most people's digestive systems with no concern; however, elderly people and people who have narrow areas in their intestines because of disease or surgery may be at risk of injury. Health Canada is monitoring the company's recall and will update the public if any new health risks are identified.
What you should do
- Stop using the recalled product. Contact your health care practitioner if you have used this product and have concerns about your health. Follow municipal or regional guidelines on how to dispose of chemicals and other hazardous waste; or Return the product to your local pharmacy for proper disposal
- Follow municipal or regional guidelines on how to dispose of chemicals and other hazardous waste; or
- Return the product to your local pharmacy for proper disposal
- Contact GSK Consumer Healthcare (doing business as Haleon) by calling 1-888-788-8181, or by emailing mystory.ca@haleon.com, if you have questions about this recall.
- Report any health product adverse events or complaints to Health Canada.
Additional official information
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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