Joint I, 60 capsules per bottle

Recall F-0931-2017 · Published 2017-01-04

Official-information notice / 官方信息说明: This page transcribes fields from the named agency record. It is not medical, legal, or food-safety advice. Follow the agency's original notice and instructions.

Recall number / 召回编号

F-0931-2017

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

Joint I, 60 capsules 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 lot and expiration date: Lot # 140115 Exp. Date 01/18

Product quantity / 产品数量

36 Bottles (12,400 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.

Open official source ↗ / 打开官方来源

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