FDA Food EnforcementMedium / 中

Magnun Plus, (30 per bottle)

Recall F-0939-2017Published 2017-01-04Company Sunset Natural Products Inc.

Reason / 召回原因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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

Distribution / 销售地区Products distributed to Florida, Nevada and the Dominican Republic

Code information / 批次信息As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lots and expiration dates: Lot # 210514 Exp. Date 05/17, Lot # 050315 Exp. Date 03/18

Official-information notice / 官方信息说明
This page organizes fields from the named agency record. It is not medical, legal, or food-safety advice. Always compare your package with the official notice.

Official record details

官方记录详情：以原始机构公告为准

Recall number / 召回编号

F-0939-2017

Classification / 风险等级

Medium / 中

Published / 发布时间

2017-01-04

Recalling firm / 召回企业

Sunset Natural Products Inc.

Product description / 产品描述

Magnun Plus, (30 per bottle)

Product code / 产品代码

Not provided in the official record

Code information / 批次与代码信息

As persuant to the Consent Decree, the firm agreed to "recall and destroy, under FDA's supervision, in accordance with the procedures provided in paragraph 6, ALL dietary supplements that were manufactured, prepared, processed, packed, labeled, held and/or distributed between April 2, 2014 and the date of entry of this Decree." The Decree was entered on September 25, 2015. Known lots and expiration dates: Lot # 210514 Exp. Date 05/17, Lot # 050315 Exp. Date 03/18

Product quantity / 产品数量

900 Bottles (27,000 capsules)

Distribution / 销售地区

Products distributed to Florida, Nevada and the Dominican Republic

Reason for recall / 召回原因

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 manufactured or distributed since April 2, 2014, hire a cGMP expert and receive written permission from FDA to resume operations.

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Last synchronized: 2026-08-09. Recall Radar does not replace agency guidance.