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

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

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 ...

By Denise Mann HealthDay ReporterTUESDAY, July 22, 2025 (HealthDay News) — More than 67,000 cases of Power Stick deodorant have been recalled due to an undisclosed manufacturing issue.

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.

The U.S. Food & Drug Administration announced the ongoing recall of multiple varieties of deodorant. Keep reading to learn ...

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

A.P. Deauville has pulled over 67,000 cases of Power Stick deodorant from stores across the country after the FDA flagged issues with the product’s manufacturing process. The recall began on […] The ...

More than 67,200 Power Stick deodorants have been recalled due to manufacturing violations, according to the U.S. Food and ...