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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskCPSC
Medications & Supplements/Over-the-Counter

GSK Consumer Health Recalls Five Excedrin Brands Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

Agency Publication Date: December 23, 2020
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Summary

GSK Consumer Healthcare has recalled approximately 433,600 bottles of five different Excedrin pain relief products because the plastic bottles may have a hole in the bottom. These products contain aspirin and acetaminophen, and a hole in the bottle allows children to access the medication, bypassing the child-resistant closure and posing a risk of poisoning. The recall includes various sizes of Excedrin Migraine, Extra Strength, PM Headache, and Tension Headache sold nationwide between March 2018 and September 2020. No injuries have been reported, and consumers with affected bottles can contact GSK for a full refund.

Risk

A manufacturing defect can cause a hole to form in the bottom of the medicine bottle, allowing children to potentially access and swallow the medication. This poses a significant poisoning risk as the products contain aspirin and acetaminophen, which are hazardous if ingested by children in unregulated amounts.

What You Should Do

  1. Immediately store all Excedrin bottles out of the sight and reach of children.
  2. Inspect the bottom of your Excedrin Migraine, Extra Strength, PM Headache, or Tension Headache bottles to determine if there is a hole.
  3. If you find a hole in the bottle, stop using it and contact GSK Consumer Relations at 800-468-7746 from 8 a.m. to 6 p.m. ET Monday through Friday to receive a prepaid shipping label for a full refund.
  4. If your bottle does not have a hole, you may continue to use the product as directed.
  5. Visit www.excedrin.com and click on the 'safety issue' banner at the top of the page for more information and a full list of discontinued products.
  6. For additional questions, contact the CPSC Hotline at 800-638-2772.

Your Remedy Options

💰Full Refund

Consumers should immediately store the recalled Excedrin bottles out of sight and reach of children and inspect the bottom of the bottle to determine if there is a hole. If there is a hole in the bottle, contact GSK Consumer Relations for information on how to receive a prepaid shipping label for return to receive a full refund. Bottles without a hole can be retained and used as directed.

Contact: GSK Consumer Relations at 800-468-7746 from 8 a.m. to 6 p.m. ET Monday through Friday, or online at www.excedrin.com and click on the “safety issue” banner at the top of the page for more information.

Affected Products

Product: Excedrin Migraine Caplets (50, 80, 100, 125, 200, 250, 300-count)
Date Ranges: March 2018 - September 2020
Product: Excedrin Migraine Geltabs (50, 80, 100, 125, 200, 250, 300-count)
Date Ranges: March 2018 - September 2020
Product: Excedrin Extra Strength Caplets (50, 80, 100, 125, 200, 250, 300-count)
Date Ranges: March 2018 - September 2020
Product: Excedrin PM Headache Caplets (50, 80, 100, 125, 200, 250, 300-count)
Date Ranges: March 2018 - September 2020
Product: Excedrin Tension Headache Caplets (50, 80, 100, 125, 200, 250, 300-count)
Date Ranges: March 2018 - September 2020

Product Images

Recalled Excedrin with hole in the bottom of the bottle

Recalled Excedrin with hole in the bottom of the bottle

Recalled Excedrin Migraine Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Migraine Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Migraine Geltabs (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Migraine Geltabs (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Extra Strength Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Extra Strength Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin PM Headache Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin PM Headache Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Tension Headache Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Recalled Excedrin Tension Headache Caplets (50, 80, 100, 125, 200, 250 and 300-count)

Additional Information

Agency: Consumer Product Safety Commission (CPSC)
Recall ID: 21057
Status: Active
Manufacturer: GSK Consumer Healthcare, of Warren, N.J.
Sold By: Pharmacies, department stores, grocery stores, and hypermarkets nationwide and online from March 2018 through September 2020 for between $7 and $18.
Manufactured In: United States
Units Affected: About 433,600
Distributed To: Nationwide
Contact: GSK Consumer Relations at 800-468-7746 from 8 a.m. to 6 p.m. ET Monday through Friday, or online at www.excedrin.com and click on the “safety issue” banner at the top of the page for more information.
Agency Last Updated: December 23, 2020

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: CPSC Notice · Raw API Response