vitafusion Fiber Well 220ct recall
vitafusion Fiber Well 220ct, 10 / 220 CT
Why was vitafusion Fiber Well 220ct recalled?
Potential presence of a metallic mesh material in products.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
- Product
- vitafusion Fiber Well 220ct, 10 / 220 CT
- Recalling firm
- Church & Dwight Co., Inc. OGI Distribution Center
- Quantity
- 2928 Bottles
- Distribution
- The product was distributed thru out the US and Canada, Panama, China,
- Recall date
- May 5, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (food)