Church & Dwight Co., Inc. has voluntarily recalled all lots of three swab products due to possible fungal contamination in the cotton swab components. The recall affects Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs, and Orajel Baby Teething Swabs distributed across the United States and Puerto Rico.
The contamination poses a serious health risk. According to the recall notice, using these swabs could cause life-threatening blood infections, especially in individuals with compromised nasal mucosa caused by inflammation or injury. Children, people with weakened immune systems, and those with underlying medical conditions face the highest risk.
The recalled products include:
- Zicam Cold Remedy Nasal Swabs (UPC 732216301205), a zinc-free homeopathic cold remedy swab
- Zicam Nasal AllClear Swabs (UPC 732216301656), a nasal cleansing swab discontinued in December 2024
- Orajel Baby Teething Swabs (UPC 310310400002), pre-moistened swabs for soothing teething discomfort in infants
So far, no illnesses or adverse events have been reported in connection with these products.
Consumers who have any of the recalled swabs should stop using them immediately. They can either discard the swabs or contact Church & Dwight for a full refund by visiting www.churchdwightrecall.com or calling 800-981-4710, Monday through Friday from 9 a.m. to 5 p.m. ET.
If you suspect any health issues related to these swabs, seek medical attention promptly. Additionally, adverse reactions should be reported to the FDA’s MedWatch program online or by calling 800-332-1088.
This recall is conducted in cooperation with the U.S. Food and Drug Administration to ensure consumer safety. All other Zicam and Orajel products, including Zicam RapidMelts, are not affected by this recall.
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