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, 10. 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-0462-2021
- 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 220ct, 10 / 220 CT
Where it was distributed
The product was distributed thru out the US and Canada, Panama, China,
Questions about this recall
Is vitafusion Fiber Well, 10 recalled?
Yes. Church & Dwight Co., Inc. OGI Distribution Center recalled vitafusion Fiber Well, 10 on 19 Apr 2021. The recall is Class II and its status is Terminated. Recall number F-0462-2021.
Why was it recalled?
Potential presence of a metallic mesh material in products.
Which lots are affected?
Product Code: 027917019840 Lot Codes: WA03087520, WA02487524, WA03086273
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Church & Dwight Co., Inc. OGI Distribution Center
All 6Other Other recalls
All 4,664| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS I | Alfalfa, Net Weight 50 lbs. bag, Product of USA, International recalledAlfalfa | International Sprout Holdings | Salmonella | 17 states |
| Food | CLASS I | Crown Farms Dried Suri Cut, 200 gm per, keep frozen recalledCrown | Euro Foods Group USA NJ | Foreign Material | 4 states |
| Food | CLASS I | Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic recalledItem | Ron's Home Style Foods | Salmonella | AR, OK, TX |
| Food | CLASS I | Food to Live Organic SuperGrass Powder recalled by Lexunder | Lexunder | Salmonella | 40 states |
| Food | ANNOUNCED | Epinephrine Injection, USP 30 mg/ (1 mg/mL) multi dose vial recalledAmerican Regent, Inc. | American Regent | Particulate Matter | Nationwide |