vitafusion Fiber Well 90ct, 4/3 Pack 90CT
FDA Recall #F-0463-2021 — Class II — April 19, 2021
Product Description
vitafusion Fiber Well 90ct, 4/3 Pack 90CT
Reason for Recall
Potential presence of a metallic mesh material in products.
Recalling Firm
Church & Dwight Co., Inc. OGI Distribution Center — North Brunswick, NJ
Classification
Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Product Type
Food
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.