An urgent nationwide recall has been issued for several over-the-counter cold medications due to fears they could cause fatal fungal infections. The Food and Drug Administration (FDA) has advised consumers to stop using Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs, and Orajel Baby Teething Swabs immediately. According to the manufacturer, Church & Dwight Co., these products may be contaminated with fungi, which can lead to serious and life-threatening blood infections.
The contamination poses a significant risk, especially to children and individuals with compromised immune systems or other underlying medical conditions. The FDA warns that the fungi can enter the body through the nasal swabs and potentially travel to the brain, causing severe infections. Although no illnesses or deaths have been reported yet, the recall is a precautionary measure to prevent potential health risks.
Consumers are urged to dispose of the affected products, specifically Zicam products with lot numbers 732216301205 and 732216301656, and Orajel products with lot number 310310400002. They can also contact the manufacturer for a full refund. The recalled products were distributed across the United States and Puerto Rico. While Zicam Nasal AllClear Swabs were discontinued in December 2024, other Zicam and Orajel products remain safe for use.
The FDA emphasizes the importance of adhering to the recall to avoid any health complications. For further information or assistance, consumers can contact Church & Dwight Co. directly.
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