FindMyRecallSubscribe
Class II: temporary or reversible health riskTerminated

Sunset Natural Products Moinsage Recall

Moinsage, 60 capsules per bottle

Sunset Natural Products Inc. · Miami, FL

Risk level
Class II
Reported by FDA
Feb 24, 2016
Recall ID
F-0539-2016
Check your lot numberHow we source this data

Summary

Sunset Natural Products recalled Moinsage starting Oct 5, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0539-2016 on Feb 24, 2016. Reason: Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations. Status: Terminated.

Why it was recalled

Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Product description

Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products

Lot numbers, UPCs & expiration codes

Lot # 030615 Exp. Date 07/18 UPC 897666001164

Where it was sold

FL and NV

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-0539-2016
Classification
Class II
Status
Terminated
Recall initiated
Oct 5, 2015
FDA report date
Feb 24, 2016
Quantity
5,000 bottles (300,000 caps)
Recall type
FDA Mandated
Recalling firm
Sunset Natural Products Inc.

Original FDA data

Every field from FDA enforcement report F-0539-2016, exactly as published.

Show all FDA fields
City
Miami
State
FL
Status
Terminated
Country
United States
Event ID
72877
Address
7345 SW 45th St
Code information
Lot # 030615 Exp. Date 07/18 UPC 897666001164
Postal code
33155-4509
Report date
Feb 24, 2016
Product type
Food
Recall number
F-0539-2016
Classification
Class II
Recalling firm
Sunset Natural Products Inc.
Product quantity
5,000 bottles (300,000 caps)
Termination date
Apr 10, 2017
Reason for recall
Pursuant to a consent decree that prohibits the company and its owners for marketing dietary supplements until they, among other things, recall and destroy the dietary supplements that have been manufatured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.
Voluntary / mandated
FDA Mandated
Product description
Moinsage, 60 capsules per bottle. Manufactured by Sunset Natural Products
Distribution pattern
FL and NV
Recall initiation date
Oct 5, 2015
Initial firm notification
Other
Center classification date
Feb 17, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0539-2016, published Feb 24, 2016. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions.

How we source and update recall data · Report incorrect information

Other recent food recalls