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FDA and A.P. Deauville Recall Over 67,000 Cases of Power Stick Roll-On Deodorant

Consumers must check FDA-listed lot numbers to identify affected products for return or safe disposal.

Deodorant Recalled
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The FDA says the recall was prompted by violations of current good manufacturing practices (cGMP) - a legal set of standards companies must follow to ensure product safety.
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Overview

  • An FDA enforcement report issued July 16 lists specific lot numbers for the over 67,000 recalled Power Stick roll-on deodorant cases.
  • The recall covers three varieties: Power Stick for Her Powder Fresh (21,265 cases), Invisible Protection Spring Fresh (22,482) and Original Nourishing Invisible Protection (23,467).
  • Recalled products sold nationwide through Walmart, Dollar Tree and Amazon must be taken out of use before return or safe disposal under FDA guidance.
  • The FDA attributed the recall to deviations from Current Good Manufacturing Practice regulations at A.P. Deauville’s Easton, Pennsylvania facility without detailing precise lapses.
  • No health incidents have been reported, though the recall underscores the importance of strict manufacturing controls in personal care products.