ZICAM NASAL ALLCLEAR — Class I drug recall D-0505-2025
Ongoing recall by Church & Dwight Inc, reported 2025-07-09, distributed nationwide. Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
| Recall number | D-0505-2025 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Church & Dwight Inc, Princeton, NJ, United States |
| Recall initiated | 2025-06-06 |
| Classified | 2025-07-03 |
| Reported by FDA | 2025-07-09 |
| Distributed | Nationwide (US) |
| Quantity | 13,632 cartons |
| Reason classes | microbial contamination, sterility |
| Pathogens | mold |
| UPC / GTIN / UDI-DI | 00732216301656 |
Product
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
Reason for recall
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
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-0505-2025. 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.