FDA Food EnforcementMedium / 中

Yaco Capsules, bulk capsules

Recall F-0977-2017Published 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 # 470414 Exp. Date 05/17, Lot # 420714 Exp. Date 10/17, Lot # 020914 Exp. Date 11/17, Lot # 231214 Exp. Date 12/17, Lot # 470414 Exp. Date 12/17, Lot # 420714 Exp. Date 01/18, Lot # 020914 Exp. Date 01/18, Lot # 231214 Exp. Date 03/18, Lot # 470414 Exp. Date 04/18, Lot # 420714 Exp. Date 05/18, Lot # 020914 Exp. Date 06/18, Lot # 231214 Exp. Date 06/18, Lot # 470414 Exp. Date 09/18, Lot # 420714 Exp. Date 07/18, Lot # 020914 Exp. Date 08/18

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-0977-2017

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

Yaco Capsules, bulk capsules

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 # 470414 Exp. Date 05/17, Lot # 420714 Exp. Date 10/17, Lot # 020914 Exp. Date 11/17, Lot # 231214 Exp. Date 12/17, Lot # 470414 Exp. Date 12/17, Lot # 420714 Exp. Date 01/18, Lot # 020914 Exp. Date 01/18, Lot # 231214 Exp. Date 03/18, Lot # 470414 Exp. Date 04/18, Lot # 420714 Exp. Date 05/18, Lot # 020914 Exp. Date 06/18, Lot # 231214 Exp. Date 06/18, Lot # 470414 Exp. Date 09/18, Lot # 420714 Exp. Date 07/18, Lot # 020914 Exp. Date 08/18

Product quantity / 产品数量

3,900,000

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.