Church & Dwight Co., Inc. has announced a voluntary nationwide recall of all lots within expiry of the following products due to potential microbial contamination:
- Zicam® Cold Remedy Nasal Swabs (UPC 732216301205)
- Zicam® Nasal AllClear Swabs (UPC 732216301656)
- Orajel™ Baby Teething Swabs (UPC 310310400002)
The company stated that the recall was prompted by the identification of fungal contamination in the cotton swab components. Use of contaminated swabs could pose health risks, particularly to children, individuals with compromised immune systems, or those with nasal injuries, potentially leading to serious or life-threatening infections.
No serious adverse events related to the affected products have been reported to date.
The recalled items were distributed across the United States and in Puerto Rico. The Zicam® Nasal AllClear Swabs were discontinued in December 2024.
Consumers are advised to stop using the recalled products immediately. Refunds can be requested through www.churchdwightrecall.com or by calling Church & Dwight Consumer Relations at 1-800-981-4710, Monday through Friday, 9 a.m. to 5 p.m. ET.
Adverse reactions or quality concerns can be reported to the FDA’s MedWatch program online or via mail/fax by calling 1-800-332-1088.
This recall does not affect other Zicam or Orajel products, including Zicam RapidMelts.
The recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
