A notice posted on the Food and Drug Administration website states that the New Jersey company Church & Dwight Co., Inc. has issued a recall on several of its vitafusion gummies due to possible exposure to metallic mesh material. The recall came after an investigation by the company of two consumer reports which identified the possible presence of a metallic mesh material. Metallic mesh material, in severe cases could lead to damage of the digestive tract.
Products being recalled include:
• Vitafusion Kids Melatonin, 50 count, UPC 0-2791-00170-8, lot code WA03076268, expiration date November 2022
• Vitafusion Fiber Well, 220 count, UPC 0-27917-01984-0, lot code WA03087520, expiration date November 2022; lot code WA02487524, expiration date September 2022; and lot code WA03086273, expiration date November 2022
• Vitafusion SleepWell, 250 count, UPC 0-27917-02524-7, lot code WA03077414, expiration date November 2022
• Vitafusion MultiVites, 150 count, UPC 0-27917-01919-2, lot code WA03044959, expiration date April 2022
• Vitafusion Melatonin, 44 count, UPC 0-27917-28011-0, lot code WA03076270, expiration date November 2022
• Vitafusion Melatonin, 140 count, UPC 0-27917-02671-8; lot code WA03076990, expiration date November 2022; lot code WA03077852, expiration date November 2022; and lot code WA02608988, expiration date September 2022
• Vitafusion Fiber Well, 90 count, UPC 0-27917-01890-4, lot code WA02187020, expiration date August 2022; lot code WA03086671, expiration date November 2022; and lot code WA03087521, expiration date November 2022
If you purchased one of the recalled products, please contact us to discuss your legal options.