Vitafusion SleepWell Recalled for Potential Metallic Mesh Presence
Church & Dwight is recalling Vitafusion SleepWell due to the potential presence of a 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 Vitafusion SleepWell 250ct / 24 / 250 CT. The recall is due to the potential presence of a metallic mesh material in the products.
The product was distributed throughout the US and Canada, Panama, and China. The specific product code is 0-27917-02524-7 and the lot code is WA03077414. The quantity involved is 120 bottles.
Consumers should check their inventory for the specific product code and lot code listed above. If they have this product, they should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- vitafusion SleepWell 250ct / 24 / 250 CT
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 120
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 (1)
- Product Code: 0-27917-02524-7 Lot Codes: WA03077414
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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