Zicam,⁣ Orajel Swabs ‌Recalled Over Fungal contamination Risk

⁢ ⁣ Updated June 12, 2025
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Certain Zicam and Orajel swab products ⁢are being recalled across the U.S. ‌due to possible‍ fungal contamination, according to ‌the Food and Drug Administration (FDA). The recall was initiated by the ​manufacturer,Church &‌ Dwight Co., after identifying the issue through routine testing.

The company linked the contamination to the cotton components used ‌in the nasal swabs ⁣and ⁢ baby teething swabs. The ‍FDA advises⁣ consumers to‌ stop using the⁤ recalled⁤ products‌ immediately to avoid potential health risks.

the recall includes the following products:

• Zicam Cold Remedy Nasal Swabs (UPC 732216301205), all lots
• Zicam Nasal AllClear swabs⁢ (UPC 732216301656), all lots
• Orajel Baby Teething Swabs (UPC 310310400002), all lots

The FDA clarified that othre Zicam and Orajel products are not affected ⁣by this⁤ recall and remain safe for use.

Fungal contamination in Zicam and Orajel ‌products could lead to infections, particularly in children, individuals with compromised immune systems, or those with pre-existing medical conditions. In rare instances, the FDA warned, it‌ could result in ⁢life-threatening blood infections.

As of yet, there have been no ​reported cases of⁣ illness⁣ or serious injury related to the recalled swabs.

Consumers who have purchased the recalled items can visit ​www.churchdwightrecall.com⁢ or call (800) 981-4710 to request a full refund.

What’s next

Church & Dwight co. is working with the FDA to ‍ensure the recalled products are removed from the market. The company is also investigating the source of the contamination to prevent future occurrences.