Alert
Bo Ying Compound by Eu Yan Sang (Hong Kong) Ltd: FDA/CDER Statement – Risk of Lead Poisoning
This is a reprint of an FDA Alert. AUDIENCE: Consumer, Health Professional, Pediatrics, Family Practice ISSUE: FDA warns parents and caregivers not to use “Bo Ying compound” manufactured by Eu Yan Sang (Hong Kong) Ltd. due to the potential lead poisoning risk associated with the product. FDA learned of this risk from the New York…
[...]Regeneca Worldwide, A Division Of Vivaceuticals, Inc Voluntarily Recalls RegeneSlim Appetite Control Capsules Due To The Presence Of DMAA That May Pose Possible Health Risk
This is a reprint of an FDA Alert. Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact Consumer/Media: 949-281-2600 FOR IMMEDIATE…
[...]FDA warns consumers about potential health risks from using Thorne Research’s Captomer products
This is a reprint of an FDA Alert. [6/12/14] The U.S. Food and Drug Administration is warning consumers not to purchase or to use Thorne Research’s Captomer or Captomer-250, marketed as a dietary supplement for heavy metal toxicity and heavy metal chelation therapy. The products list DMSA (meso-2, 3-dimercaptosuccinic acid), as an active ingredient, which…
[...]Nano Well-being Health Inc. Issues Voluntary Nationwide Recall of Super Arthgold Due to Undeclared Ingredients
This is a reprint of an FDA Alert. Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact:Consumer:1-714-515-4600nanowellbeingh@gmail.com FOR IMMEDIATE RELEASE –…
[...]FDA Alert: Nova Products, Inc. Issues Voluntary Nationwide Recall of Dietary Supplements with Undeclared Active Pharmaceutical Ingredients
This is a reprint of an FDA Alert. Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact Consumer: 610-459-7709 Media:…
[...]FDA Alert: Pure Edge Nutrition, LLC Issues Voluntary Nationwide Recall of Bella Vi Brand Products Due to Undeclared Sibutramine and Phenolphthalein
This is a reprint of an FDA Alert. Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact Consumer: (888) 417-3613 info@pureedgenutrition.com…
[...]FDA Alert: Glaxosmithkline Recalls Alli®
This is a reprint of an FDA Alert Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact: Consumer: 800-671-2554 Media:Deborah Boldingdeborah.g.bolding@gsk.com412-327-5540 FOR…
[...]FDA Alert: SNI National is Voluntarily recalling Kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack Due to Undeclared Drug Ingredients
This is a reprint of an FDA Alert. Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact: Consumer: 1-801-388-4690 Kratomrecall@gmail.com Media:…
[...]FDA Alert: New Life Nutritional Center Issues Voluntary Nationwide Recall of Super Fat Burner, Maxi Gold and Esmeralda Dietary Supplements Due to the Presence of Undeclared Sibutramine and Phenolphthalein
Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact Consumer: 646-209-9846 rosadohow@aol.com Media: Nilson Rosado 646-209-9846 FOR IMMEDIATE RELEASE – March…
[...]FDA Alert: Pain Free by Nature is Voluntarily Recalling Reumofan Plus Tablets Due to Undeclared Drug Ingredients
This is a reprint of an FDA Alert Recall — Firm Press Release FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. Contact Consumer: 719-235-8864 Media: 719-235-8864…
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