Recalls / Class I
Class ID-0505-2025
Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.
Product
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
- Affected lot / code info
- All Lots.
Why it was recalled
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
Recalling firm
- Firm
- Church & Dwight Inc
- Notification channel
- Press Release
- Type
- Voluntary: Firm initiated
- Address
- 469 N Harrison St, Princeton, New Jersey 08540-3510
Distribution
- Quantity
- 13,632 cartons
- Distribution pattern
- Nationwide in the USA.
Timeline
- Recall initiated
- 2025-06-06
- FDA classified
- 2025-07-03
- Posted by FDA
- 2025-07-09
- Status
- Ongoing
Source: openFDA Drug Enforcement endpoint. Recall record D-0505-2025. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.