Church & Dwight Co., Inc. Zicam Cold Remedy Medicated Nasal Swabs Recall
Recall affects Zicam Cold Remedy Medicated Nasal Swabs distributed nationwide in the United States. The recall is due to CGMP deviations after FDA inspection found out-of-spec microbiological testing results at the contract manufacturer. The affected lots are UN52882 (04/30/2028), UN53431 (06/30/2028), and UN60411 (08/31/2028).
| Brand | Church & Dwight Co., Inc. |
|---|---|
| Product | Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205. |
| Reason | CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing |
| Severity | moderate |
| Units affected | 318600 |
| Distribution | US Nationwide. |
| Agency | FDA |
WHAT YOU SHOULD DO
- Stop using recalled Zicam Medicated Nasal Swabs from lots UN52882, UN53431, and UN60411.
- Check the lot numbers on your package and dispose of or return any affected product according to retailer instructions.
- Contact Church & Dwight Co., Inc. for recall instructions, refunds, or replacements, or visit the FDA recall page for details.
- If you have health concerns after using the product, consult your doctor.
How to identify the recalled item
| Lot / date codes | Lot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028. |
|---|---|
| Lot / date codes | Lot # UN52882, Exp Date: 04/30/2028; Lot # UN53431, Exp Date: 06/30/2028; Lot # UN60411, Exp Date: 08/31/2028. |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.