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  2. Hyland's - Wikipedia

    en.wikipedia.org/wiki/Hyland's

    [6] [7] Hyland's began selling a reformulated version of the product with a child proof cap in 2011. [8] In 2016, Hyland's indicated it would stop selling its Hyland's Teething Tablets product in the U.S. [9] after the FDA claimed it received reports of 10 child deaths and 400 adverse effects associated with the product.

  3. Hyland's Teething Tablets recalled over potentially toxic ...

    www.aol.com/news/2010-10-26-hylands-teething...

    Hyland's Teething Tablets are being recalled because they contain belladonna, a controlled substance that could be toxic to children, the U.S. Food and Drug Administration said. ... The recall was ...

  4. Homeopathic baby tablets linked to poisonings finally recalled

    www.aol.com/article/news/2017/04/17/homeopathic...

    A line of products suspected of poisoning hundreds of children and killing several has finally been recalled by its manufacturers after years of warnings.

  5. Evidence and efficacy of homeopathy - Wikipedia

    en.wikipedia.org/wiki/Evidence_and_efficacy_of...

    On September 30, 2016, the FDA issued a safety alert to consumers [127] warning against the use of homeopathic teething gels and tablets following reports of adverse events after their use. The agency recommended that parents discard these products and "seek advice from their health care professional for safe alternatives" [ 128 ] to homeopathy ...

  6. U.S. Consumer Product Safety Commission - Wikipedia

    en.wikipedia.org/wiki/U.S._Consumer_Product...

    old Logo. The United States Consumer Product Safety Commission (USCPSC, CPSC, or commission) is an independent agency of the United States government.The CPSC seeks to promote the safety of consumer products by addressing "unreasonable risks" of injury (through coordinating recalls, evaluating products that are the subject of consumer complaints or industry reports, etc.); developing uniform ...

  7. Drug recall - Wikipedia

    en.wikipedia.org/wiki/Drug_recall

    Drug recall. A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug ...

  8. Feds warn against some baby loungers, cradle swings ... - AOL

    www.aol.com/feds-warn-against-baby-loungers...

    Separately, owners of DNYSYSJ and OUKANING cradle swings are being cautioned against their use after an infant's death in a crib of similar design, bringing the total number of deaths to six, the ...

  9. 2010 Johnson & Johnson children's product recall - Wikipedia

    en.wikipedia.org/wiki/2010_Johnson_&_Johnson...

    The 2010 Johnson & Johnson children's product recall involved 43 over-the-counter children's medicines announced by McNeil Consumer Healthcare, a subsidiary of Johnson & Johnson, on April 30, 2010. Medications in the recall included liquid versions of Tylenol, Tylenol Plus, Motrin, Zyrtec, and Benadryl. The products were recalled after it was ...