Moringa Premium 60 capsules
Recalled by Borinquen Natural on Sep 9, 2013
Recall Summary
Borinquen Natural recalled Moringa Premium 60 capsules in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Sep 9, 2013.
The FDA-published reason for this recall is: "Distributed dietary supplements with the following claims in the firm's website: "prevents depression, hypertension, renal diseases, arthritis, cancer, diabetes, obesity, heart conditions, etc.""
Distribution was limited; the FDA record lists "PR only." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Carolina, PR. The recall covers 1418, total for all varieties of product. The FDA has Terminated this recall (first reported Dec 11, 2013), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.
Reason for Recall
Distributed dietary supplements with the following claims in the firm's website: "prevents depression, hypertension, renal diseases, arthritis, cancer, diabetes, obesity, heart conditions, etc."
Product Description
Moringa Premium 60 capsules
Distribution
PR only.
What Should You Do?
- 1.Check your kitchen for this product immediately.
- 2.Do not consume the recalled product.
- 3.Return the product to where you bought it for a full refund, or throw it away.
- 4.If you have experienced any health issues, contact your healthcare provider.
Browse Related Recalls
Terms Explained
- Class II Recall — learn what this means in food safety
- FDA Food Recall — learn what this means in food safety
Source: FDA Recalls, Market Withdrawals and Safety Alerts, 2026.