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FDA Publishes Lot Numbers in Ongoing Power Stick Deodorant Recall

Consumers now have a detailed list of affected lot numbers to confirm whether their roll-on deodorants are included in the recall.

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

  • The recall covers 67,214 cases of Power Stick roll-on deodorants flagged for cGMP deviations.
  • The affected batches include 21,265 cases of Power Stick for Her (Powder Fresh), 22,482 cases of Invisible Protection (Spring Fresh) and 23,467 cases of Original Nourishing roll-ons.
  • A. P. Deauville voluntarily launched the recall on July 10 after FDA inspectors identified manufacturing practice lapses at its Easton, Pennsylvania facility.
  • Affected products were distributed nationwide through Walmart, Dollar Tree and Amazon.
  • No injuries have been reported and consumers should stop using recalled items and follow FDA guidance on returning or securely disposing of affected products.