Church & Dwight recalls select Zicam and Orajel swab products over contamination concerns

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Sara Brenner, Acting Commissioner of Food and Drugs | U.S. Food and Drug Administration

Church & Dwight recalls select Zicam and Orajel swab products over contamination concerns

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Church & Dwight Co., Inc. has announced a voluntary recall of specific swab products due to potential microbial contamination. The affected items include Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs, and Orajel Baby Teething Swabs. The contamination involves fungi found in the cotton swab components, posing a risk to consumer health.

The company warns that contaminated swabs could lead to severe health issues, including serious blood infections, especially in children and those with weakened immune systems or pre-existing conditions. However, no adverse events have been reported so far.

The recalled products were distributed across the United States and Puerto Rico. Details for each product are as follows:

- Zicam Cold Remedy Nasal Swabs (UPC 732216301205): A zinc-free homeopathic remedy intended to reduce cold duration.

- Zicam Nasal AllClear Swabs (UPC 732216301656): A nasal cleansing product discontinued in December 2024.

- Orajel Baby Teething Swabs (UPC 310310400002): Pre-moistened swabs for soothing teething discomfort in infants.

Consumers are advised to stop using these products immediately and contact Church & Dwight's Consumer Relations team for refunds or further information via their website or at (800) 981-4710 during business hours.

Reports of adverse reactions can be submitted through the FDA's MedWatch Adverse Event Reporting program online or by mail/fax. This recall is being conducted with FDA oversight.

It is important to note that this recall only affects specific Zicam and Orajel swab products; other items like Zicam RapidMelts remain unaffected.

For more information about Church & Dwight Co., Inc., visit their official website.

Media inquiries can be directed to Keith Walsh at keith.walsh@edelman.com.

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