Vitafusion Fiber Well Recalled for Potential Metallic Mesh Presence
Church & Dwight is recalling Vitafusion Fiber Well bottles due to the potential presence of metallic mesh material in the product.
The agency’s classification
FDA (Food): Class II
Class II is 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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (foreign object) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
Church & Dwight Co., Inc. is recalling 2,928 bottles of Vitafusion Fiber Well 220ct. The recall is due to the potential presence of a metallic mesh material in the products.
The affected product is identified by Product Code 027917019840 and Lot Codes WA03087520, WA02487524, and WA03086273. The product was distributed throughout the US and Canada, Panama, and China.
Consumers should check their inventory for the specific lot codes listed above. If the product is found, consumers should stop using it and follow instructions from the recalling firm or the FDA.
The recalled product
- Product
- vitafusion Fiber Well 220ct, 10 / 220 CT
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 2,928
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Product Code: 027917019840 Lot Codes: WA03087520
- WA02487524
- WA03086273
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 6 recalled by Church & Dwight Co., Inc. OGI Distribution Center under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 6 products in this recall →Related recalls
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