Class I · Most seriousActive recall
ZICAM COLD REMEDY MEDICATED NASAL SWABS
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberAll lots.
Where it was soldNationwide in the USA.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Church & Dwight Co,. Inc., Ewing NJ. UPC 7 32216 30120 5 |
Show the full FDA record
| Full product label | 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 |
| Distribution | Nationwide in the USA. |
| Quantity | 3,374,918 cartons |
| Recall initiated | 2025-06-06 |
| Report date | 2025-07-09 |
| Recall completed | — |
| Recall number | D-0504-2025 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Princeton NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.