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can be found at a Web page set up to provide information about the McNeil Product Recall?”

mcneil Product recall web page
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can be found at a Web page set up to provide information about the McNeil Product Recall?”

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A recall of Tylenol Arthritis Pain Caplet 100-count bottles started in November has been expanded to include about 500 lots of other popular over-the-counter drugs, the FDA announced today. Affected are certain lots of various adult and children’s Tylenol products, Motrin IB tablets and caplets, Benadryl Allergy tablets, Rolaids antacid tablets, Simply Sleep mini-caplets, and St. Joseph chewable and safety-coated aspirin, all made by McNeil Consumer Healthcare. Not all of the lots have been linked to consumer complaints of “an unusual, moldy, musty, or mildew-like odor,” but they all have the potential to be affected, according to the company. Specific lot numbers affected by the recall can be found at a Web page set up to provide information about the McNeil Product Recall. The FDA urged McNeil to perform a thorough investigation into the complaints, which eventually resulted in the expanded voluntary recall. By law, the FDA cannot force a company to withdraw products. In a small numb

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A recall of Tylenol Arthritis Pain Caplet 100-count bottles started in November has been expanded to include about 500 lots of other popular over-the-counter drugs, the FDA announced today. Affected are certain lots of various adult and children’s Tylenol products, Motrin IB tablets and caplets, Benadryl Allergy tablets, Rolaids antacid tablets, Simply Sleep mini-caplets, and St. Joseph chewable and safety-coated aspirin, all made by McNeil Consumer Healthcare. Not all of the lots have been linked to consumer complaints of “an unusual, moldy, musty, or mildew-like odor,” but they all have the potential to be affected, according to the company. Specific lot numbers affected by the recall can be found at a Web page set up to provide information about the McNeil Product Recall. The FDA urged McNeil to perform a thorough investigation into the complaints, which eventually resulted in the expanded voluntary recall. By law, the FDA cannot force a company to withdraw products. In a small numb

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