Vitafusion Fiber Well 220ct (Church & Dwight) – Metallic Mesh (2021)
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
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
vitafusion Fiber Well 220ct, 10 / 220 CT
Brand
Church & Dwight Co., Inc. OGI Distribution Center
Lot Codes / Batch Numbers
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
Products Sold
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
Church & Dwight Co., Inc. OGI Distribution Center is recalling vitafusion Fiber Well 220ct, 10 / 220 CT due to Potential presence of a metallic mesh material in products.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential presence of a metallic mesh material in products.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026