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Class II: temporary or reversible health riskTerminated

Borinquen Natural Moringa Premium 60 capsules Recall

Moringa Premium 60 capsules

Borinquen Natural · Carolina, PR

Risk level
Class II
Reported by FDA
Dec 11, 2013
Recall ID
F-0692-2014
Check your lot numberHow we source this data

Summary

Borinquen Natural recalled Moringa Premium 60 capsules starting Sep 9, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0692-2014 on Dec 11, 2013. Reason: Distributed dietary supplements with the following claims in the firm's website: "prevents depression, hypertension, renal diseases, arthritis, cancer, diabetes, obesity, heart conditions, etc.". Status: Terminated.

Why it was recalled

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

Lot numbers, UPCs & expiration codes

none

Where it was sold

PR only.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0692-2014
Classification
Class II
Status
Terminated
Recall initiated
Sep 9, 2013
FDA report date
Dec 11, 2013
Quantity
1418, total for all varieties
Recall type
Voluntary: Firm initiated
Recalling firm
Borinquen Natural

Original FDA data

Every field from FDA enforcement report F-0692-2014, exactly as published.

Show all FDA fields
City
Carolina
State
PR
Status
Terminated
Country
United States
Event ID
66343
Address
1265 Calle Marginal Villamar STE 3
Address (line 2)
Urb. Villamar
Code information
none
Postal code
00979
Report date
Dec 11, 2013
Product type
Food
Recall number
F-0692-2014
Classification
Class II
Recalling firm
Borinquen Natural
Product quantity
1418, total for all varieties
Termination date
Apr 26, 2017
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."
Voluntary / mandated
Voluntary: Firm initiated
Product description
Moringa Premium 60 capsules
Distribution pattern
PR only.
Recall initiation date
Sep 9, 2013
Initial firm notification
Visit
Center classification date
Dec 3, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0692-2014, published Dec 11, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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