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Product Review
Astaxanthin Supplements Review
See Which Astaxanthin Products Passed or Failed CL's Tests
News Release
March 13, 2006
ConsumerLab.com reports on supplements for bone health containing calcium and vitamin D— Results posted for 32 supplements for adults and children; One found contaminated with lead
WESTCHESTER COUNTY, NEW YORK — MARCH 13, 2006 — ConsumerLab.com announced test results today from its new Product Review of Supplements for Bone Health covering 32 adult and children's products containing calcium and vitamin D. Sales of calcium supplements in the U.S.
News Release
June 10, 2003
ConsumerLab.com finds lead in coral calcium product; Product also charged with false advertising by FTC — Calcium supplement product review published online today
WHITE PLAINS, NY — June 10, 2003 — (Updated August 8) — ConsumerLab.com today reported finding problems among the calcium products recently tested in its Product Review of Calcium Supplements.
News Release
May 20, 2003
Consumers advised to read labels carefully when selecting herbal supplements for prostate — Saw palmetto product review published online today
WHITE PLAINS, NY — May 20, 2003 — ConsumerLab.com reported today that only two-thirds of the saw palmetto supplements it recently evaluated contained ingredients similar to those known to work in clinical studies.
Recalls & Warnings
June 04, 2004
FTC Charges Marketers of Two Supplements with False Claims to Cure Range of Diseases
On June 3, 2004 the Federal Trade Commission (FTC) charged marketers of two dietary supplements with falsely claiming that their products can prevent and cure cancer and other diseases. According to the FTC’s complaint, Boston-area marketers Direct Marketing Concepts, Inc. (DMC), ITV Direct, Inc.
Recalls & Warnings
August 31, 2009
Court Orders Marketers of Supreme Greens and Coral Calcium to Pay Nearly $70 Million for Consumer Refunds
On August 27, 2009, a federal district court ordered the marketers of two dietary supplements – "Supreme Greens" and "Coral Calcium" – who claimed the products would cure ailments ranging from cancer and Parkinson’s disease to heart disease and autoimmune diseases to pay nearly $70 million for ...
Recalls & Warnings
January 23, 2025
Glutathione Distributor Warned by FDA
On November 13, 2024, the FDA issued a Warning Letter to Western Innovations, Inc.
Recalls & Warnings
March 13, 2020
FDA Finds Problems at 52% of Supplement Manufacturing Sites in U.S. and 42% Abroad
ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2019 (October 1, 2018 - September 30, 2019) of 598 dietary supplement manufacturing facilities in the U.S.
Recalls & Warnings
July 26, 2023
Gadget Island, Inc. Male Enhancement Supplements Found to Contain Prescription Drugs
On July 21, 2023, the FDA issued a warning letter to Gadget Island, Inc.
Recalls & Warnings
September 21, 2023
Moor Herbs, Inc Warned for Manufacturing Violations, Drug Claims
On August 1, 2023, the FDA issued a Warning Letter to Moor Herbs, Inc.
Recalls & Warnings
January 04, 2024
Toxic Herb Found in More Tejocote Root Supplements
On January 3, 2024, the FDA warned consumers not to purchase or use certain tejocote root supplements after FDA laboratory analysis confirmed the products contain yellow oleander (Thevetia peruviana), a toxic herb.
Recalls & Warnings
October 06, 2005
Deceptive Marketing of “Supreme Greens" -- Settlement with FTC
On October 6, 2005, the Federal Trade Commission (FTC) announced that three individuals and two companies have settled FTC charges over their roles in the deceptive marketing of Supreme Greens, an herbal supplement.
Recalls & Warnings
September 12, 2006
U.S. Marshalls Seize Supplements Promoted as Drugs
On September 6, 2005, the U.S. Food and Drug Administration (FDA) announced that, at its request, U.S. Marshals seized quantities of Ellagimax capsules, Coral Max capsules, Coral Max without Iron capsules, and Advanced Arthritis Support capsules distributed by Advantage Nutraceuticals L.L.C.
Recalls & Warnings
May 30, 2017
Seller of Vitamin C, Calcium, Mushroom Supplements and More Warned for Manufacturing Violations
On May 12, 2017 the FDA issued a warning letter to VitaPurity Corporatio.
Recalls & Warnings
September 01, 2022
Elite One Source Nutritional Services Warned for Manufacturing, Labeling Violations
On August 5, 2022, the FDA issued a warning letter to dietary supplement manufacturer Nutritional Laboratories International, Inc. (DBA Elite One Source Nutritional Services, Inc.
Recalls & Warnings
December 29, 2022
EarthLab, Inc. Warned for Promoting Curcumin, Elderberry to Treat Pain & Flu
On November 10, 2022, the FDA issued a warning letter to EarthLab, Inc., dba Wise Woman Herbals following inspection of the company’s website which found statements about the company’s products to be drug claims because they suggest the products can prevent or treat disease.
Recalls & Warnings
May 04, 2023
FDA Warns MedoLife for Promoting Homeopathic Products to Treat COVID-19, Cancer
On April 19, 2023, the FDA issued a warning letter to Medolife Rx D/B/A MedoLife Corp., AELIA Inc. and Queanta Inc.
Recalls & Warnings
September 10, 2021
FDA Warns Ten Sellers of "Diabetes" Supplements
On September 7, 2021, the FDA issued warning letters to 10 supplement companies that made drug claims by promoting products to treat diabetes and/or lower blood sugar. Five of the products were sold on Amazon as well as on company websites. The products were promoted with statements such as
Recalls & Warnings
May 23, 2013
Seller of Sexual Enhancement, Cholesterol, Resveratrol Supplements and More Warned For Drug Claims
On May 2, 2013, the FDA issued a warning letter to Alternative Health Supplements, following a review of the company's website, which found statements made about several dietary supplements, including Regenerect, Alligin, Astaxanthin Advantage, HDL Cholesterol Management, Resveratrol, Coral Calcium ...
Recalls & Warnings
June 19, 2008
FDA Warns Groups to Stop Selling Fake Cancer 'Cures'
On June 17, 2008, the FDA reported that it had sent Warning Letters to 23 U.S. companies and two foreign individuals marketing a wide range of products fraudulently claiming to prevent and cure cancer.
Recalls & Warnings
August 27, 2013
Immune Supplement Recalled Due To Undeclared Milk
On August 23, 2013, Reaction Nutrition, LLC issued a voluntary recall of immune support supplement LIVE CLINICAL 90 CAPS because it contains undeclared milk.
Recalls & Warnings
April 17, 2021
NS NY Distributor Inc Male Enhancement Products Recalled Due to Undeclared Drugs
On April 8, 2021, NS NY Distributor Inc issued a recall of all lots of Premium Orgazen 7000 and Ginseng Power 5000 male enhancement capsules because FDA analysis found them to contain sildenafil and/or tadalafil.
Recalls & Warnings
April 28, 2020
Ten Multi-Level Marketing Companies Warned for Coronavirus and Deceptive Earnings Claims
On April 24, 2020, the FTC announced that it sent warning letters to ten multi-level marketing companies for selling products such as essential oils and immune system boosters with unsupported claims that they can treat coronavirus (COVID-19) and/or for misrespresenting potential earnings people ...
Recalls & Warnings
March 20, 2020
Seller of Rejuvenation Pills Settles Charges of Making False Claims
Health Center, Inc. has agreed to halt their allegedly deceptive advertising claims about three "cure-all" health and wellness products that targeted older consumers nationwide after the Federal Trade Commission (FTC) filed a complaint.
Recalls & Warnings
March 12, 2016
FDA Finds Problems at 58% of Supplement Manufacturing Sites in U.S. and Abroad
ConsumerLab.com has obtained results of the FDA's inspections in Fiscal Year 2015 (ending September 30) of 483 dietary supplement manufacturing facilities, showing that most -- 58.2% -- received letters indicating noncompliance with current Good Manufacturing Practices (cGMPs).
Recalls & Warnings
September 11, 2015
Thirteen Manufacturers Ordered to Stop Selling Devil's Claw Supplements
On September 9, 2015, the New York State Attorney General ordered 13 manufacturers, including Thorne Research Inc., NBTY, Inc. (Puritan's Pride) Inc., and Now Foods, to stop selling devil's claw supplements which were found to contain the incorrect species of the plant.
Recalls & Warnings
April 09, 2003
Recall of Dangerous Sexual Enhancement Supplement Illegally Containing Viagra Ingredient
On April 4, 2003, the U.S. Food and Drug Administration's MedWatch program announced that Ultra Health Laboratories, Inc. and Bionate International, Inc. are warning consumers not to purchase or consume a product known as Vinarol tablets.
Recalls & Warnings
April 25, 2017
Beware of Products Which Promise to Treat or Cure Cancer, FDA Warns
On April 25, 2017, the FDA warned consumers to be aware of supplements and other products claiming to cure cancer.
Recalls & Warnings
October 15, 2012
Recall of Nutrition Bars Containing Peanut Butter Due To Salmonella Risk
On October 11 and 12, 2012, four brands of nutrition bars were voluntarily recalled due to possible salmonella contamination of the peanut butter used in each of these bars. The peanut butter was produced by Sunland Inc., and is part of a larger recall of Sunland's peanut butter and peanut products.
Recalls & Warnings
February 29, 2008
FTC Sues Sellers of Weight-Loss Pills for False Advertising
On February 8, 2008 the The Federal Trade Commission (FTC) charged a business operation with violating federal law by falsely claiming that its weight-loss pills cause users to lose weight without dieting or exercise.
Recalls & Warnings
March 31, 2005
FDA Warns Marketer of "Vitamin O" Product to Cease Unsubstantiated Claims
The U.S. Food and Drug Adminstration (FDA) has sent a Warning Letter (dated February 8, 2005) to Donald L. Smyth, President, R-Garden Inc., and Rose Creek Health Products, Inc. warning that its "Vitamin O" product was, among other things, being marketed with unsubstantiated health claims.
Recalls & Warnings
January 18, 2002
Recall of Pepsin-containing Digestive Supplements
The U.S. Food and Drug Administration (FDA) released the following Class I recall information in its January 16, 2002 Enforcement Report.
Recalls & Warnings
August 02, 2012
FDA Warns Two Supplement Makers of Manufacturing Violations
On July 19, 2012, the FDA issued a warning letter to H & L Jerch Sales, Inc. for failing to maintain written quality control procedures, which constitutes a violation of current Good Manufacturing Practices (cGMP) and caused the company’s products to be declared adulterated.
Recalls & Warnings
July 05, 2012
FDA Warns Good Herbs Inc. of Manufacturing Violations and Drug Claims
The FDA issued a warning letter to Good Herbs Inc. on May 24, 2012, after a facility inspection found the company to be in violation of current manufacturing regulations, including lack of documentation and written procedures.
Recalls & Warnings
January 10, 2013
FDA Warns Aloe and Herbal Supplement Companies For Manufacturing Violations
AloeScience Labs, Inc. -- On November 14, 2012, the FDA issued a warning letter to AloeScience Labs, Inc.
Recalls & Warnings
March 14, 2011
22 Brands of Whey Protein Recalled Due to Salmonella Concern
The FDA posted a recall notice involving 22 brands of whey protein powder due to potential contamination with salmonella. The recall was voluntarily initiated on March 10, 2011 by the manufacturer of the products, Vitalabs, Inc.
Recalls & Warnings
November 15, 2009
Nationwide Recall of a Weight Loss Supplement Found to Contain Undeclared Drug Ingredients
On November 12, 2009, The U.S. Food and Drug Administration (FDA) announced that it informed GMP Herbal Products, Inc. that its product "Pai You Guo," a weight loss dietary supplement, contains undeclared drug ingredients.
Recalls & Warnings
December 17, 2004
FDA Seizes Ginseng Because of Potentially Risky Pesticide Residues
On December 16, 2004, the Food and Drug Administration (FDA) announced that the U.S. District Court for the District of New Jersey issued a warrant for the seizure of imported ginseng held for sale at FCC Products, Inc., located in Livingston, N.J. The U.S.
Recalls & Warnings
October 12, 2005
Supplement Company to Pay $2 Million Penalty For Alleged Violations of FTC Order
On October 12, 2005 the Federal Trade Commission (FTC) announced that under the terms of a consent decree approved by the it for submission by the U.S. Department of Justice (DOJ) to the federal court for approval, NBTY, Inc. (NBTY, formerly Nature’s Bounty, Inc.
Recalls & Warnings
April 19, 2007
Recall of Another Sex Enhancement Supplement
On April 17, 2007 the Food and Drug Administration (FDA) website posted an announcement that Jen-On Herbal Science International, Inc. is conducting a voluntary nationwide recall of the company's supplement product sold under the name H S Joy of Love. Jen-On Herbal Science International, Inc.
Recalls & Warnings
August 11, 2015
Company Ordered to Stop Making and Selling Supplements
On August 4, 2015, a federal court ordered a permanent injunction against dietary supplement company Atrium Inc., and two companies under the same ownerhship, Aspen Group Inc., Nutri-Pak of Wisconsin Inc.
Recalls & Warnings
February 01, 2018
Seller of Supplements for Opiate Withdrawal Warned for Drug Claims
On January 11, 2018, the FDA sent warning letters to ten sellers of supplements promoted to treat opiate withdrawal following reviews of the companies' websites and social media which found statements and testimonials made about the products to be drug claims.
Recalls & Warnings
January 02, 2012
FDA Warns XYMOGEN of Manufacturing and Labeling Violations Regarding Multiple Products
On December 13, 2011, the U.S. FDA sent a Warning Letter to Atlantic Pro Nutrients, Inc. (dba XYMOGEN) regarding labeling and/or manufacturing violations relating to its products, which include Borage CP-240, CoQmax CF, Immune Rx, Iron Glycinate, and Green Tea 600.
Recalls & Warnings
October 06, 2011
Testosterone Booster Supplement Recalled for Containing Synthetic Steroid
On October 5, 2011, the U.S. FDA announced that Superior Metabolic Technologies Inc of Marietta, Georgia is voluntarily recalling all lots of the testosterone booster Uprizing 2.
