The US Food and Drug Administration (FDA) has recalled cases of deodorant due to deviations from manufacturing regulations ...

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Over 67,000 cases of these products have been recalled by the manufacturer from stores across the country. Consumer should check their cabinets now.

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The FDA has recalled over 67,000 cases of deodorant sold nationwide due to CGMP deviations. Three types of Power Stick ...

The FDA did not provide a reason for the recall, but said the products had a cGMP (Current Good Manufacturing Practices) ...

More than 67,000 cases of roll-on deodorant that were sold nationwide have been voluntarily recalled due to an undisclosed ...

The FDA and Power Stick recalled thousands of deodorant cases because manufacturing practices did not comply with FDA ...

According to a public notice published by the federal Food & Drug Administration (FDA), over 67,000 cases of Power Stick deodorant items — which are manufactured by Easton, Pennsylvania-based A.P.

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.