FDA Drugs recall ·
ZICAM COLD REMEDY MEDICATED NASAL SWABS, 20 Single-Use Swabs per carton… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0504-2025
- Date
- (initiated June 6, 2025)
- Company / brand
- Church & Dwight Inc
469 N Harrison St, Princeton, NJ, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 3,374,918 cartons
- Hazard tags
- Sterility Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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
Why was it recalled?
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All lots.
Distribution
Nationwide in the USA.
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0504-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.