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Karma, bulk capsules

FDA Recall #F-0970-2017 — Class II — October 13, 2015

Recall #F-0970-2017 Date: October 13, 2015 Classification: Class II Status: Terminated

Product Description

Karma, bulk capsules

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

Recalling Firm

Sunset Natural Products Inc. — Miami, FL

Classification

Class II — A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.

Product Type

Food

Status

Terminated

Voluntary / Mandated

FDA Mandated

What Should You Do?

Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.

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