Public recall detail

TUMS Peppermint Regular Strength tablets: One lot recalled due to contamination

2022-11-30

high
Recall Safety notice
Quick summary

Quick summary: TUMS Peppermint Regular Strength tablets: One lot recalled due to contamination. Date: 2022-11-30.

Recommended action

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.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandTUMS
ProductTUMS Peppermint Regular Strength tablets, packages of three rolls of 12 tablets, lot HA7H, NPN 01970240
IssueHealth products - Contamination Health products - Product safety
IdentificationRA-72300

Affected products

ProductTUMS Peppermint Regular Strength (500mg) tablets, packages of three rolls of 12 tablets
DIN / NPN / authorization01970240
LotHA7H
CodesAugust 2027

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
AudienceIdentification number RA-72300
CategoryHealth products - Natural health products
CompaniesPublished by Health Canada
Published byHealth Canada
Alert / recall typePublic advisory
Identification numberRA-72300
Background{}
CompaniesPublished by Health Canada
AudiencesIdentification number RA-72300
Source updated2022-11-30

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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