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.
What this means for you
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 (metallic mesh in a supplement) where injury has not yet been reported, fitting the High severity criteria.
Plain-English summary
Church & Dwight Co., Inc. is recalling 7,782 bottles of Vitafusion Fiber Well 90ct, 4/3 Pack 90CT. The recall is being conducted because of the potential presence of a metallic mesh material in the products.
The affected product was distributed throughout the US and Canada, Panama, and China. The specific lot codes involved are WA02187020, WA03086671, and WA03087521. The product code is 027917018904.
Consumers should check their inventory for these specific lot codes and stop using the product if it matches the recalled items.
The recalled product
- Product
- vitafusion Fiber Well 90ct, 4/3 Pack 90CT
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 7,782
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: 027917018904 Lot Codes: WA02187020
- WA03086671
- WA03087521
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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