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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Zicam, Orajel swab products recalled, Hawaii health officials say | Honolulu Star-Advertiser
Hawaii Department of Health officials alerted residents today of a recall of some Zicam and Orajel brand products due to potential microbial contamination of their cotton swabs.
·Honolulu, United States
Read Full Article'Contaminated' cupboard staple recalled over 'life-threatening fungi'
A HOUSEHOLD must-have has been urgently pulled from shelves after officials discovered it could contain dangerous fungus. The contaminated swabs can lead to serious and possibly deadly infections. GettyConsumers are urged to stop using the products immediately (stock image)[/caption] WRALThe recalled products have been sold nationwide across the US and Puerto Rico[/caption] The recall has affected products sold across the US and Puerto Rico. New…
·New York, United States
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