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Consumers across the United States are being urged to stop using specific Zicam® and Orajel™ swab products after the FDA announced a nationwide recall due to fungal contamination in their cotton swab components. The recall includes all lot numbers of Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs, and Orajel Baby Teething Swabs. These products were distributed across the country, including Puerto Rico, and are now at the center of growing public concern.
Fungal contamination in medical or over-the-counter products is not a minor issue—it presents a very real risk of infection. When fungal organisms come into contact with damaged nasal or oral tissue, they can enter the bloodstream and lead to severe, and sometimes life-threatening, conditions such as systemic fungal infections. Vulnerable populations—including infants, individuals with weakened immune systems, or anyone with open nasal wounds or oral inflammation—are particularly susceptible.
These products were marketed as safe remedies for common ailments like colds and teething discomfort. But when safety is compromised by microbial contamination, the results can be devastating. Consumers who trusted these brands now face potential health complications that could have been entirely preventable.
If you or a loved one used one of these recalled swabs and experienced any unusual symptoms, infections, or required medical treatment, you may have grounds for a product liability claim. Our law firm is actively investigating these incidents and pursuing legal action for affected individuals.
Church & Dwight Co., Inc., the manufacturer of both brands, issued a voluntary recall for three swab-based products due to the presence of fungal contamination in the cotton components. These products were sold nationwide and used by both adults and infants.
Here are the affected products:
All expiration dates and lot numbers of these products are affected. This is a full consumer-level recall.
This recall does not include other Zicam or Orajel products such as RapidMelts, but the inclusion of infant products in this recall raises significant concern about the manufacturer’s quality control practices.
Swabs contaminated with fungus can pose serious health threats. The recall was initiated after it was discovered that the swabs may expose users to fungal microbes capable of causing infections, especially in individuals with open wounds, inflamed nasal passages, or compromised immune systems. Infants and toddlers, particularly those using the Orajel Baby Teething Swabs, face the highest level of risk.
Potential health consequences include:
Medical complications arising from fungal contamination can require prolonged treatment, including antifungal medication, hospitalization, and ongoing medical supervision. For infants, the risks are especially concerning due to their undeveloped immune systems and inability to communicate early symptoms.
Consumers who used the affected products and later suffered from infections or related health issues should speak with a product liability lawyer immediately. A claim could help recover compensation for medical expenses, pain and suffering, and other damages.
Manufacturers have a legal responsibility to ensure their products are safe for consumer use, especially when those products are intended for infants or are used in sensitive areas like the nose and mouth. When this duty is violated, and people are harmed as a result, the legal system provides a path for justice and financial recovery.
Victims may be entitled to compensation for:
Product liability lawsuits also serve a broader purpose—they help hold corporations accountable and push for higher safety standards across the industry. By filing a claim, you are not only seeking justice for yourself or your child but helping prevent similar harm from occurring to others.
Our law firm is investigating claims nationwide and is prepared to pursue litigation against Church & Dwight Co., Inc. on behalf of individuals harmed by these dangerous products.
If you used one of the recalled swabs and later experienced any signs of infection, fever, swelling, nasal pain, teething complications, or had to seek medical treatment, you may have a valid legal claim. This is especially important if the user was an infant or someone with an existing health condition.
Even if you’re unsure whether your symptoms are connected, it is worth discussing with a qualified product liability lawyer who can help assess the situation and determine next steps.
Do not discard the product packaging or swabs if they are still available—preserving evidence could support your case. Also keep records of any medical care received, including prescriptions, doctor visits, ER records, and bills related to treatment.
Parker Waichman LLP is a national law firm with decades of experience handling high-stakes product liability cases involving dangerous drugs, defective medical devices, and hazardous consumer products. Our legal team understands the physical, emotional, and financial toll these situations create.
We are accepting cases across the United States from individuals and families impacted by the recalled Zicam and Orajel products. Whether your child suffered a teething-related infection or you experienced complications from using a cold remedy swab, we can help pursue the justice you deserve.
There are time limits to file a claim, so it’s important to take action as soon as possible.
If you or your child suffered a fungal infection or medical complication after using Zicam® Cold Remedy Nasal Swabs, Zicam® AllClear Swabs, or Orajel™ Baby Teething Swabs, you may be eligible for compensation. Parker Waichman LLP is currently accepting cases nationwide. Don’t wait to take action—call now for your free legal consultation at 1-800-YOUR-LAWYER (1-800-968-7529). Our product injury lawyers will review your case and explain your rights. You pay nothing unless we win your case.
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