August 2026 FDA Recall Drug by Church & Dwight Co., Inc.
D-0790-2026 - CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing

This Class II drug recall was voluntarily initiated by Church & Dwight Co., Inc. on August 10, 2026 for the product Drug. The FDA reported the reason for recall as cgmp deviations; fda inspection of the contract manufacturer noted out of limit results for microbiological testing. The product was distributed Nationwide and the recall is currently ongoing.

Recall Number: D-0790-2026

Reason for Recall
CGMP Deviations; FDA inspection of the contract manufacturer noted out of limit results for microbiological testing
Initiated
08-10-2026
Reported
09-02-2026
Quantity
318,600 cartons

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Church & Dwight Co., Inc.
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.

Batch or Lot Expiration Information

Lot# UN52882, Exp Date: 04/30/2028
Lot# UN53431, Exp Date: 06/30/2028
Lot# UN60411, Exp Date: 08/31/2028.