CLASS II Food recall · Reported 5 May 2021 · FDA Enforcement Report
vitafusion Fiber Well recalled by Church & Dwight Co., Inc. OGI
Church & Dwight Co., Inc. OGI Distribution Center is recalling vitafusion Fiber Well. The recall was initiated on 19 Apr 2021 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0463-2021
- FDA event ID
- 87745
- Recalling firm
- Church & Dwight Co., Inc. OGI Distribution Center, North Brunswick, NJ
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 19 Apr 2021
- FDA classified
- 28 Apr 2021
- Reported
- 5 May 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 19 Apr 2021 | Recall initiated by company | |
| 28 Apr 2021 | Classified by FDA | +9 days |
| 5 May 2021 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential presence of a metallic mesh material in products.
Product as listed by the FDA
vitafusion Fiber Well 90ct, 4/3 Pack 90CT
Where it was distributed
The product was distributed thru out the US and Canada, Panama, China,
Questions about this recall
Why was it recalled?
Potential presence of a metallic mesh material in products.
Which lots are affected?
Product Code: 027917018904 Lot Codes: WA02187020, WA03086671, WA03087521
Where was it sold?
The product was distributed thru out the US and Canada, Panama, China,
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
5 other products · FDA event 87745This product is part of a recall event; the main page for the event is vitafusion Melatonin vitafusion Melatonin recalled.
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