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

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 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 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 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)

Name of Product:
Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets
Hazard:

Some of the bottles containing the over-the-counter drug can have a hole in the bottom.  If there is a hole, children could access and swallow the contents, posing a risk of poisoning.  These products contain the substances aspirin and acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA).

Remedy:
Refund
Recall Date:
December 23, 2020
Units:

About 433,600

Consumer 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.

Recall Details

Description:

This recall involves 50, 80, 100, 125, 200, 250 and 300-count bottles of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets.  The bottles are plastic with a child-resistant closure.  For a full list of the recalled products, visit www.excedrin.com/products/discontinued.

Remedy:

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.

Incidents/Injuries:

None reported.

Sold At

Pharmacies, department stores, grocery stores, and hypermarkets nationwide and online from March 2018 through September 2020 for between $7 and $18.

Manufacturer(s):

GSK Consumer Healthcare, of Warren, N.J.

Manufactured In:
United States
Recall number:
21-057
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About the U.S. CPSC
The U.S. Consumer Product Safety Commission (CPSC) is charged with protecting the public from unreasonable risks of injury or death associated with the use of thousands of types of consumer products. Deaths, injuries, and property damage from consumer product incidents cost the nation more than $1 trillion annually. CPSC’s work to ensure the safety of consumer products has contributed to a decline in the rate of deaths and injuries associated with consumer products over the past 40 years. Federal law bars any person from selling products subject to a publicly announced voluntary recall by a manufacturer or a mandatory recall ordered by the Commission.
For lifesaving information:
SaferProducts.gov