FDA recalls more than 4 million tubes of toothpaste
The agency identifies it as a Class II recall, which describes cases when product usage or exposure may cause temporary health issues.
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The Food and Drug Administration has issued a nationwide recall of more than four million tubes of toothpaste.
The agency identifies it as a Class II recall, which describes cases when product usage or exposure may cause temporary health issues.
“Current Good Manufacturing Practice deviations” is listed as the reason on the FDA website.
The CGMP is a system of regulations and guidelines ensuring products are held to high quality standards.
The recall impacts 17 different varieties of toothpaste, including some marketed toward children.
Click here to view a full list.
