WASHINGTON, DC—Church & Dwight Co. is recalling all lots of Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs, and Orajel Baby Teething Swabs due to potential fungal contamination in the cotton swab components, the U.S. Food and Drug Administration has announced.
The FDA warned that swabs containing microbial contamination could pose a significant health risk, including serious and life-threatening blood infections, particularly for users with compromised nasal passages. The risk is highest for children and individuals with weakened immune systems or other underlying medical conditions.
The recalled products were distributed throughout the United States and Puerto Rico.
Church & Dwight Co. stated that, to date, no serious adverse events have been reported in connection with the recalled products.
The recall is limited to Zicam and Orajel swab products only. Other Zicam and Orajel products, such as Zicam RapidMelts, are not affected.
Consumers who have purchased any of the recalled products are advised to stop using them immediately. Full refunds are available by visiting www.churchdwightrecall.com or by calling the Consumer Relations team at (800) 981-4710.
The recalled products include:
- Zicam Cold Remedy Nasal Swabs (all lots): A zinc-free, homeopathic cold remedy designed to shorten the duration of the common cold.
- Zicam Nasal AllClear Swabs (all lots): A nasal cleansing swab product that was discontinued in December 2024.
- Orajel Baby Teething Swabs (all lots): Pre-moistened swabs intended to soothe teething discomfort in infants and toddlers.
Health care professionals and patients are encouraged to report any adverse events or side effects related to the use of these products to the FDA’s MedWatch Safety Information and Adverse Event Reporting Program. Reports can be submitted online, by downloading a form or by calling 1-800-332-1088.
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