Recalls & Safety Records

Warning letterFDA · Sep 7, 2017

Newton Everett/WR Group Inc. 9/7/17

Named company: Newton Everett/WR Group Inc.

A drug is misbranded under section 502(f)(1) of the Act [21 U.S.C. 352(f)(1)] if the drug fails to bear adequate directions for its intended use(s). Accordingly, your products fail to bear adequate directions…

Warning letterFDA · Sep 1, 2017

Nd Labs, Inc. 9/1/17

Named company: Nd Labs, Inc.

Based on the inspection and review of the product labels you provided during the inspection, we have found serious violations of the Federal Food, Drug, and Cosmetic Act (the Act) and applicable regulations as…

Warning letterFDA · Aug 30, 2017

MusclMasster, LLC 8/30/17

Named company: MusclMasster, LLC

Based on the inspection, a review of the product labels collected during the inspection, and a review of your website at www.thegreenherb.com, we have identified serious violations of the Federal Food, Drug,…

These results describe the included collection. Sources and coverage.