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FDA recalls over 67,000 cases of Power Stick deodorant

Here’s what you should know about the 67,000 cases of deodorant being recalled

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

Deodorant recall linked to violations. Here's which ones and why

A.P. Deauville, a Pennsylvania-based health and beauty manufacturer, has recalled more than 67,000 cases of its Power Stick roll-on deodorants.

Austin American-Statesman on … · 12h

FDA recalls over 67,000 cases of Power Stick deodorant due to manufacturing violations

On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good Manufacturing Practice (CGMP) standards, a set of FDA-enforced guidelines designed to ensure product safety and quality.

ConsumerAffairs13h

Recall issued for 67,000 cases of deodorant

Over 67,000 cases of “Power Stick” roll‑on deodorant recalled by A.P. Deauville due to cGMP violations. Three variants are ...

Green Matters on MSN1h

Popular Deodorant Brand Recalls Over 67,000 Cases of Antiperspirant for Failing To Reach Quality and Safety Standards

The FDA is sounding the alarm with a deodorant recall that is impacting more than 67,000 cases of antiperspirant made by a ...

7hon MSN

Deodorant recall shocker! These everyday brands just failed major safety tests - is your brand on the list?

A.P. Deauville recalled over 67,000 cases of Power Stick roll-on deodorants. The recall happened because the products did not ...

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