Church & Dwight Co., Inc. has recalled all lots of its over-the-counter products 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 recall was announced on June 6, 2025 and affects all lots within expiration dates distributed in the United States and Puerto Rico. (fda.gov)
Why the Recall Matters
The recall stems from the discovery of microbial contamination, identified as fungi, in the cotton swab components of these products. While the specific type of fungi has not been disclosed, the contamination poses a significant health risk, particularly to children and individuals with compromised immune systems or underlying medical conditions. Using these contaminated swabs could lead to serious and potentially life-threatening blood infections, especially in users whose nasal mucosa may be compromised due to inflammation or mechanical injuries. (USATODAY, The Hill)
Affected Products
The following products are included in the recall:
- Zicam Cold Remedy Nasal Swabs
UPC: 732216301205
A zinc-free, homeopathic cold remedy swab designed to shorten the duration of the common cold. - Zicam Nasal AllClear Swabs
UPC: 732216301656
A nasal cleansing swab product (discontinued in December 2024). - Orajell Baby Teething Swabs
UPC: 310310400002
Pre-moistened swabs designed to soothe teething discomfort in infants and toddlers.
What Consumers Should Do
If you have purchased any of the affected products, it is crucial to take the following steps:
- Stop Using the Products Immediately
Discontinue use of the recalled swabs to prevent potential health risks. - Dispose of the Products Safely
Do not use or share the swabs. Dispose of them according to local guidelines. - Request a Refund
Visit www.churchdwightrecall.com or contact Church & Dwight’s Consumer Relations team at (800) 981-4710 for a full refund.
The company is offering full refunds and is coordinating the recall with FDA oversight. To date, no serious adverse events associated with the affected products have been reported.
Stay Informed
This recall adds to a series of recent product recalls. Consumers are advised to stay informed about product recalls and safety alerts by regularly checking the FDA’s recall alerts: FDA Recall Alerts
If you or a loved one were injured by a recalled product, contact Goldenberg Lauricella at (612)-333-4662 for a free consultation. Our team has the expertise and knowledge to help you get the justice you deserve.