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Cold Remedy Nasal Swabs, Nasal AllClear Swabs, Baby Teething Swabs Recall Due...

# Major Recall Alert: Cold Remedy Nasal Swabs, Nasal AllClear Swabs, Baby Teething Swabs Recalled Due to Microbial Contamination

Church & Dwight Co., Inc. has issued a major recall on specific Zicam® and Orajel™ products due to microbial contamination risks. This precautionary recall highlights the potential health threats caused by contaminated cotton swab components, especially for those most vulnerable. Below, we dive into the details of this recall, steps for consumers, and how you can stay updated on important product safety concerns.

## Why This Recall is Important

This recall is critical because of the serious health risks posed by microbial contamination, specifically fungi, in the recalled products. Here’s why the issue demands attention:
- The affected products include **Zicam® Cold Remedy Nasal Swabs**, **Zicam® Nasal AllClear Swabs**, and **Orajel™ Baby Teething Swabs**, all widely used across the U.S.
- Contaminated swabs can cause severe health complications, particularly if the nasal mucosa is already inflamed or injured.
- Individuals with compromised immune systems, underlying medical conditions, or young children are at the highest risk, potentially facing life-threatening blood infections.

Although no adverse events have been reported to date, Church & Dwight Co., Inc. is acting responsibly with this voluntary recall to ensure consumer safety.

## Details of the Recall

Here’s what we know about the recall and the products involved:

- **Recalled Products**:
- Zicam® Cold Remedy Nasal Swabs (all lots within expiry)
- Zicam® Nasal AllClear Swabs (all lots within expiry)
- Orajel™ Baby Teething Swabs (all lots within expiry)
- **Reason for Recall**: Microbial contamination (fungi) in the cotton swab components.
- **Distribution**: These products were distributed across the United States—including Puerto Rico.
- **Other Zicam and Orajel Products Are Safe**: The recall applies exclusively to the swab products. Other Zicam products, such as Zicam RapidMelts, are not affected.

This recall has been issued in coordination with the **U.S. Food and Drug Administration (FDA)** to prioritize consumer safety. For more information, refer to the official [FDA recall notice](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-co-inc-issues-voluntary-nationwide-recall-zicamr-cold-remedy-nasal-swabs-zicamr-nasal).

## What You Should Do

If you’ve purchased or are using any of the recalled swab products, take the following actions immediately:

- **Stop Using the Product Now**: Discontinue use, even if you have not experienced adverse effects.
- **Request a Refund**: Visit [www.churchdwightrecall.com](http://www.churchdwightrecall.com) or contact their Consumer Relations team at **(800) 981-4710** (Monday–Friday, 9 AM–5 PM ET). A full refund is being offered.
- **Report Adverse Effects to the FDA**: If you’ve experienced any issues with these products, report them via the FDA MedWatch Adverse Event Reporting Program:
- **Online**: Submit via the FDA’s MedWatch website.
- **Mail or Fax**: Download the form or request one by calling **(800) 332-1088**. Complete and mail or fax it to **1-800-FDA-0178**.

## Stay Safe – Get Instant Recall Alerts

Your health and safety should always come first. To stay informed about product recalls like this, consider downloading our app for instant alerts on food, medication, and product safety news. With just a few taps, you can:
- Receive real-time recall notifications.
- Access detailed product safety information.
- Take quick action to protect your family's health.

[**Download the App Now**](#) and never miss an important recall update again.

### Final Thoughts

The Zicam® and Orajel™ swab recall is a critical reminder of the importance of monitoring product safety. While no adverse events have been reported yet, Church & Dwight Co., Inc.’s proactive approach prioritizes consumer care. Remember to stop using these products immediately, seek a refund, and report any issues to the FDA.

For more details about the recall, visit the official [FDA recall notice page](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/church-dwight-co-inc-issues-voluntary-nationwide-recall-zicamr-cold-remedy-nasal-swabs-zicamr-nasal). Stay informed, stay safe, and take action today.

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