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Recall of Zicam and Orajel Products: FDA

  • Church & Dwight Co., Inc. voluntarily recalled three swab products on June 6, 2025, affecting the U.S. and Puerto Rico markets.
  • The recall followed detection of possible fungal contamination in cotton components that could cause serious blood infections, especially in vulnerable users.
  • The affected products include Zicam Cold Remedy Nasal Swabs and Orajel Baby Teething Swabs, with all lots within expiry being recalled and no serious adverse events reported.
  • Consumers were urged to immediately stop using the swabs and can obtain a full refund by visiting www.churchdwightrecall.com or calling the consumer relations team at 800-981-4710.
  • This recall highlights a significant health risk to children and immunocompromised individuals and underscores the importance of product safety monitoring.
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Recall of Zicam and Orajel products: FDA

·Washington, United States
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Fungi concerns spark nationwide recall of Zicam and Orajel products

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Wral News broke the news in Raleigh, United States on Sunday, June 8, 2025.
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