Zicam Cold Remedy Medicated Nasal Swabs Recall: Sterility Concern
ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
What is the FDA recall status?
The FDA record lists this recall as ongoing. FDA enforcement data is not a live recall-lifecycle tracker. Follow the official instructions and check the agency notice or firm for current guidance.
Why was Zicam Cold Remedy Medicated Nasal Swabs recalled?
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
What should I do if I have this product?
Follow the firm and FDA instructions for the affected product. Contact the recalling firm for current guidance.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare your product with the product description and available lot, UPC or model codes below from the official FDA record to check whether it is covered by this recall. If an identifier is missing or unclear, check the complete official notice or contact the firm; an incomplete match here does not establish that your product is unaffected.
Full product description
ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
Which lot codes, UPCs or models are affected?
All lots.
- Agency record number
- D-0504-2025
- Product
- ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5
- Recalling firm
- Church & Dwight Inc
- Quantity
- 3,374,918 cartons
- Distribution
- Nationwide in the USA.
- Recall started
- June 6, 2025
- Report date
- July 9, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (drug)