Zicam — Class II drug recall D-0790-2026
Ongoing recall by Church & Dwight Co., Inc., reported 2026-09-02, distributed nationwide. CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological te
| Recall number | D-0790-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Church & Dwight Co., Inc., Ewing, NJ, United States |
| Recall initiated | 2026-08-10 |
| Classified | 2026-08-26 |
| Reported by FDA | 2026-09-02 |
| Distributed | Nationwide (US) |
| Quantity | 318,600 cartons |
| Reason classes | microbial contamination, cgmp |
| UPC / GTIN / UDI-DI | 00732216301205 |
| Lot numbers | UN52882, UN53431, UN60411 |
| Expiration dates | 2028-04-30, 2028-06-30, 2028-08-31 |
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 for recall
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0790-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.