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Baby Powder Manufacturer Voluntarily Recalls Products for Asbestos
October 18, 2019
WASHINGTON, Oct. 18 -- The U.S. Department of Health and Human Services' Food and Drug Administration issued the following news release:

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- FDA advises consumers to stop using affected products

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The U.S. Food and Drug Administration is alerting consumers of a voluntary recall by Johnson & Johnson of Johnson's Baby Powder after FDA testing has found that a sample from one lot of the product contains chrysotile fibers, a type of asb . . .

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