Church & Dwight Inc. is recalling approximately 4,084,430 cartons of Zicam and Orajel Baby swab products, including Zicam Cold Remedy Medicated Nasal Swabs, Zicam Nasal AllClear, and Orajel Baby Cooling Swabs for Teething. The recall was initiated because fungal contamination was found in the nasal and oral swabs. These products are distributed nationwide in the United States, and the recall affects all lots of the specific UPC codes listed below.
Using products contaminated with fungi can lead to serious infections, particularly in infants using oral swabs or in individuals with compromised immune systems. Using contaminated nasal swabs may lead to respiratory or sinus infections.
You have 2 options:
Recall #: D-0504-2025; Distributed by Church & Dwight Co,. Inc., Ewing NJ.
Recall #: D-0505-2025; Distributed by Church & Dwight Co,. Inc., Ewing NJ.
Recall #: D-0506-2025; Manufactured for Church & Dwight Co. Inc. Ewing. NJ 08328 USA.
Labeling, Zicam® Cold Remedy Nasal Swabs
UPC, Zicam® Cold Remedy Nasal Swabs
Labeling, Zicam® Nasal AllClear Swabs
UPC, Zicam® Nasal AllClear Swabs
Labeling, Orajel™ Baby Teething Swabs
- UPC, Orajel™ Baby Teething Swabs
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · FDA Press Release · Raw API Response
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