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

FDA findings of manufacturing deviations at Easton, Pennsylvania have prompted an ongoing probe into potential contamination risks

FDA has issued a recall involving tens of thousands of Power Stick antiperspirant deodorant cases, the recall was prompted by “cGMP deviations,
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More than 67,000 cases of various Power Stick deodorant are being recalled.

Overview

  • FDA enforcement report published July 16 lists specific lot numbers for three scented Power Stick roll-ons subject to the recall
  • The voluntary withdrawal covers 21,265 cases of the Power Fresh scent, 22,482 cases of Spring Fresh Invisible Protection and 23,467 cases of Original Nourishing roll-ons sold nationwide at Walmart, Dollar Tree and Amazon
  • The recall was triggered by violations of Current Good Manufacturing Practice standards at A. P. Deauville’s Pennsylvania factory
  • No consumer injuries have been reported to date and customers should check their product’s lot numbers against the FDA list before returning affected items for a full refund
  • A. P. Deauville initiated the recall voluntarily and continues to cooperate with the FDA’s investigation into its quality control processes