ZICAM NASAL ALLCLEAR recall — Class I (D-0505-2025) · pharmaranks
Class IOngoing
ZICAM NASAL ALLCLEAR recall
FDA recall D-0505-2025 · initiated Jun 6, 2025
Most serious — a reasonable probability that use will cause serious harm or death.
Why it was recalled
Microbial Contamination of Non-Sterile Products: Fungal contamination of nasal swabs.
Details
Product
ZICAM NASAL ALLCLEAR, 20 Single-Use Swabs per carton, Distributed by Church & Dwight Co,. Inc.., Ewing NJ. UPC 7 32216 30165 6
Recalling company
Church & Dwight Inc
Classification
Class I
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide in the USA.
Initiated
Jun 6, 2025
FDA report date
Jul 9, 2025
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.