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FDA recall, , Moderate risk

Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus

Zicam Cold Remedy Medicated Nasal Swabs have out of limit results for microbiological testing.

What happened

Church & Dwight Co., Inc., of Ewing, New Jersey, recalled Zicam Cold Remedy Medicated Nasal Swabs with Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, distributed nationwide. The FDA inspection of the contract manufacturer noted out of limit results for microbiological testing. The recall began on August 10, 2026, and was added to the FDA's Enforcement Report on August 26, 2026.

The product is identified as Zicam Cold Remedy Medicated Nasal Swabs with Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, distributed by Church & Dwight Co. Inc., Ewing, NJ 08628. The recall covers 318,600 cartons.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:

  1. Check the FDA or company notice for instructions specific to this product.
  2. Ask your pharmacist or doctor whether your lot is affected and what to do.

Is yours affected?

Match the UPC and lot code listed under your product.

A UPC is the number printed under a barcode.

  1. UPC
    • 732216301205
    Lot code
    • UN52882
    • UN53431
    • UN60411

Recall details

Company began the recall
Sold in

US Nationwide.

Company
Church & Dwight Co., Inc.Ewing, New Jersey
Risk

Moderate risk

Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
99604
Recall number
D-0790-2026
Quantity recalled
318,600 cartons

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 2, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)