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FDA · Drugs ·

Zicam recall

Church & Dwight Co., Inc. recalled Zicam on September 2, 2026 because of cGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing. It was sold nationwide.

Why it was recalled

CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing

What's recalled

Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.

Quantity: 318,600 cartons

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Church & Dwight Co., Inc., Ewing, NJ
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
US Nationwide.
Status
Ongoing
Recall number
D-0790-2026
Source
U.S. Food and Drug Administration

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