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Perrigo is a leading global consumer-focused self-care company. Our vision is to make lives better by bringing “Quality, Affordable Self-Care Products” that consumers trust everywhere they are sold. The Company is a leading provider of health and wellness solutions that enhance individual well-being by empowering consumers to proactively prevent or treat conditions that can be self-managed.

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Perrigo Company Recalls Children's Pain Reliever Suspension Liquid

Perrigo Company today announced that, in cooperation with the U.S. Food and Drug Administration (FDA), it is conducting a recall of 7,788 four-ounce bottles of cherry-flavored pain reliever suspension liquid with Lot Number 1AD0228.

Perrigo determined that this lot may contain an excess of up to 29 percent over the labeled amount of acetaminophen. The product is being recalled because overdoses of acetaminophen can lead to severe health problems including liver toxicity and liver failure.

The product, which is used to treat headaches and fevers in children, was sold under the Good Sense® label at various small independent retail chains across the country, under the Hy-Vee® label at Hy-Vee stores in Illinois, Iowa, Kansas, Minnesota, Missouri, Nebraska and South Dakota and under the Kroger® label at Kroger stores in Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Mississippi, Missouri, North Carolina, Ohio, South Carolina, Tennessee, Texas, Virginia and West Virginia.

Perrigo immediately notified the FDA as well as the retailers and wholesale distributors of this product. No consumer complaints have been reported.

Of the 7,788 bottles affected in this recall, Perrigo estimates that approximately 6,500 were purchased by consumers. The rest have been removed from retailers' shelves and inventory.

Consumers who purchased bottles with Lot Number 1AD0228, which is printed on each bottle's label and carton, are urged to discontinue use of the product immediately and return it to the place of purchase for a full refund. Consumers with questions may contact Perrigo at 1-800-321-0105.

Any adverse reactions experienced with the use of this product should also be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088, by fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 56000 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at .


SOURCE: Perrigo Company

Contact: Ernest J. Schenk, Manager, Investor Relations and Communication
of Perrigo Company, +1-616-673-9212, email,


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