vitafusion MultiVites 150ct,
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0461-2021.
Potential presence of a metallic mesh material in products.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0461-2021.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Church & Dwight Co., Inc. Ogi Distribution Center or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0461-2021.
Church & Dwight Co., Inc. OGI Distribution Center
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Church & Dwight Co., Inc. Ogi Distribution Center Recall FAQ
Church & Dwight Co., Inc. Ogi Distribution Center is the subject of a food safety report: vitafusion MultiVites 150ct,. The notice was published on April 19, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 683 units are potentially affected.