Moringa Premium 60 capsules
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0692-2014.
Distributed dietary supplements with the following claims in the firm's website: "prevents depression, hypertension, renal diseases, arthritis, cancer, diabetes, obesity, heart conditions, etc."
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0692-2014.
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 Borinquen Natural 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-0692-2014.
Borinquen Natural
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.
Borinquen Natural Recall FAQ
Borinquen Natural is the subject of a food safety report: Moringa Premium 60 capsules. The notice was published on September 9, 2013 by the U.S. Food and Drug Administration (FDA). Approximately 1,418 units are potentially affected.