Showing Results for Royal King
Filters
View All
Search term may appear only in full report available to members. Join now for full access.
Product Review
Canned Tuna, Salmon, Sardines & Mackerel Review
Find Fish With the Least Mercury & Arsenic and Most Omega-3s
CL Answer
Do any supplements help reduce menstrual pain or symptoms of premenstrual syndrome (PMS)?
Find out which supplements help reduce premenstrual syndrome (PMS) symptoms, such as mood swings, pain, bloating, irritability and food cravings.
CL Answer
How good are sardines? Are they healthy and safe? What did CL's tests find?
Find out amounts of omega-3s (DHA and EPA), protein, and vitamin D in sardines, as well as contaminants mercury and arsenic based on ConsumerLab's tests.
News Release
June 12, 2025
Best & Worst Canned Tuna, Salmon, Sardines & Mackerel
White Plains, NY, June 12, 2025 – High levels of mercury and/or arsenic were found in several popular brands of canned tuna and sardines recently tested by ConsumerLab.com.
Recalls & Warnings
April 23, 2025
FDA Warns Consumers Not to Use ADVANCED KING Joint Supplement
On February 10, 2025, the FDA warned consumers not to purchase or use the joint pain supplement ADVANCED KING (Naturista Store LLC), because FDA analysis confirmed the product contains dexamethasone, diclofenac, and methocarbamol.
Recalls & Warnings
July 13, 2022
FDA Warns Sellers of Tainted Honey-Based Sexual Enhancement Products
On July 12, 2022, the FDA issued warning letters to four companies selling honey-based products promoted for sexual enhancement after tests conducted by the FDA found the products to contain the prescription drugs Tadalafil and Sildenafil.
Recalls & Warnings
October 26, 2023
Joint Pain Supplements Recalled Due to Undeclared Drug Ingredients
On October 22, 2023, Botanical-Be recalled of all lots of the company’s Kuka Flex Forte, Artri King, and Reumo Flex capsule products after FDA laboratory analysis found them to contain undeclared diclofenac.
Recalls & Warnings
June 02, 2022
Walmart Inc. Recalls Joint Supplements With Omega-3, Glucosamine & Curcumin
On May 28, 2022, Walmart Inc. issued a voluntary recall of all lots of Artri Ajo King Joint Supplements after FDA laboratory analysis found the presence of undeclared diclofenac.
Recalls & Warnings
July 15, 2022
Honey-Based Enhancement Supplement Recalled
On July 13, 2022, Shopaax.com issued a recall of all lots of its honey-based sexual enhancement product, Kingdom Honey Royal Honey VIP, after FDA analysis found the presence of undeclared sildenafil.
Recalls & Warnings
June 16, 2022
Omega 3 Supplements Recalled Due to Undeclared Drug Ingredients
On May 28, 2022, Latin Foods Market issued a voluntary recall of one lot of Artri King Reforzado con Ortiga y Omega 3 tablets after FDA laboratory analysis found the presence of undeclared diclofenac and dexamethasone.
Recalls & Warnings
April 27, 2022
Prescription Drugs Found in Arthritis, Muscle Pain, and Osteoporosis Supplements
On April 20th, 2022, the FDA warned consumers not to use the following ”Artri“ or ”Ortiga” products promoted to treat arthritis, muscle pain, osteoporosis and bone cancer because they have been found to contain undeclared drugs that can have serious adverse ...
Recalls & Warnings
October 02, 2023
Dangerous Ingredients Found in Ten Arthritis and Pain Supplements
On September 29, 2023, the FDA warned consumers that the following arthritis and pain management products contain undeclared drugs such as diclofenac, methocarbamol (a muscle relaxant), and dexamethasone (a corticosteroid), and/or other potentially harmful ingredients.
News Release
July 10, 2020
Best and Worst Tuna, Salmon and Sardines? ConsumerLab Tests Reveal Amounts of Omega-3s and Toxic Heavy Metals in Canned and Packaged Fish
White Plains, New York, July 10, 2020 — Canned and packaged tuna, salmon and sardines can be an excellent source of omega-3 fatty acids, but some may also be contaminated with toxic heavy metals such as mercury and arsenic.
Recalls & Warnings
August 28, 2018
King Bio Homeopathic Product Recall Expanded
On August 27, 2018, King Bio expanded its initial recalls of certain homeopathic products and children's homeopathic products to include all of its aqueous-based products for human and animal use due to possible microbial contamination.
Recalls & Warnings
March 16, 2023
Omega-3 Supplements for Dogs and Cats Recalled Due to Potential for Vitamin A Toxicity
On March 9, 2023, Stratford Care USA issued a recall of 62 brands of omega-3 supplements for dogs and cats due to potentially elevated levels of vitamin A.
Recalls & Warnings
July 10, 2020
Sundial Herbal Recalls More Than Sixty Products Including Turmeric, Cinnamon & Tea
On July 9, 2020, Sundial Herbal Products issued a recall of more than 60 herbal products because they were misbranded and/ or promoted with drug claims. Their labels contain drug claims stating the products can diagnose, cure, mitigate, treat, or prevent disease.
Recalls & Warnings
July 24, 2018
Contaminated Homeopathic Products Recalled
On July 20, 2018, King Bio issued a recall of four lots of its homeopathic products Aquaflora Candida HP9, Lymph Detox, and Baby Teething liquids because they were found to contain microbial contaminants including Pseudomonas Brenneri, Pseudomonas Fluroescens and ...
Recalls & Warnings
November 18, 2003
Supplement Promoted As Cancer Treatment Removed from Market
On November 10, 2003, the Food and Drug Administration (FDA) announced that NBTY, Inc., of Bohemia, N.Y.
Recalls & Warnings
June 19, 2013
Sexual Enhancement Supplement Found To Contain Undeclared Drug
On June 17, 2013, the FDA advised consumers not to purchase or use sexual enhancement supplement Royal Dragon Herbal Tonic Balls because it was found to contain undeclared vardenafil.
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
March 30, 2019
FDA Warns Seller of Reishi, Joint Supplements, Ginseng & More for Pesticides, Other Violations
On March 12, 2019, the FDA issued a warning letter to Yanqing "Michael" Li and Chang Su, owners of the website http://www.woohoonatural.
Recalls & Warnings
August 25, 2018
Thirty-Two Children's Homeopathic Products Recalled
On August 22, 2018, King Bio issued a recall of 32 homeopathic products for children because some have have tested positive for microbial contamination.
Recalls & Warnings
September 08, 2018
Homeopathic Oral Sprays Recalled Due to Possible Bacterial Contamination
On September 5, 2018, Beaumont Bio Med, Inc., issued a recall of all of its water and alcohol-based homeopathic products because they have the potential to contain microbial contaminants.
Recalls & Warnings
June 16, 2019
"Immune Support" Throat Sprays Recalled
On June 13 2019, APS BioGroup, Inc. issued a recall of four "immune support" throat sprays because they have the potential to be contaminated with Stenotrophomonas maltophilia, a bacteria that can cause respiratory infection, particularly in individuals with weakened immune systems.
Recalls & Warnings
May 09, 2020
FTC Warns 45 More Companies for Coronavirus Claims
On May 7, 2020, the FTC announced that it sent warning letters to 45 companies for selling products such as herbal products, immune system boosters, and vitamin C with unsupported claims that they can treat coronavirus (COVID-19).
Recalls & Warnings
December 19, 2020
FDA Finds Unapproved Drugs in Many Weight Loss and Sexual Enhancement Products Sold Online
On December 18, 2020, the FDA warned consumers that certain products promoted for weight loss, body building, sexual enhancement, pain relief, sleep, and other uses because may contain harmful ingredients.
Recalls & Warnings
July 18, 2017
Hidden Drugs Found in Sexual Enhancement Products
On July 17, 2017, the FDA posted public notifications after finding multiple sexual enhancement products contained hidden drug ingredients.
Recalls & Warnings
March 08, 2012
Supplement Maker Warned About Cancer Claims
FDA issued a letter to Royal Domains (dated January 6, 2012) warning that their Nature's Pearl Premium Muscadine Grape Seed dietary supplement is being promoted as a drug and as such is misbranded.
Recalls & Warnings
June 22, 2017
FDA Finds Hidden Drug Ingredients in Sexual Enhancement Supplements
On June 22, 2017, the FDA warned consumers that the following sexual enhancement supplements were found to contain undeclared sildenafil, tadalafil and/or dapoxetine. Use the links below to read the complete warning letter for each:
- Triple Premium Zen Gold 1300 mg
Recalls & Warnings
September 17, 2013
Seller of Omega-3 and Joint Supplements Warned for Manufacturing Violations and Drug Claims
On August 29, 2013, the FDA issued a warning letter to Y.S. Health Corp.
Recalls & Warnings
March 19, 2009
QVC Settles Charges of False Claims for Supplements
On March 19, 2009, the Federal Trade Commission (FTC) announced that QVC, Inc., a TV home shopping channel and one of the world’s largest multimedia retailers, has agreed to pay $7.
Recalls & Warnings
March 21, 2017
Twenty-one Sexual Enhancement Products Recalled
On March 7, 2017, A&H Focal Inc. issued a recall of the following sexual enhancement supplements because they were found to contain drugs such as sildenafil, tadalafil, vardenafil:
Recalls & Warnings
May 02, 2015
Three Sexual Enhancement Supplements Contain Prescription Drug
On April 30, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplements listed below because they were found to contain sildenafil. Each was identified during an examination of international mail shipments:
Recalls & Warnings
March 06, 2015
Four Male Enhancement Supplements Found to Contain Drug
On March 5, 2015, the FDA warned consumers not to buy or use the following four sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
March 02, 2015
Hidden Drug Found in Six Sexual Enhancement Supplements
On February 27 and February 28, 2015, the FDA warned consumers not to buy or use the following six sexual enhancement supplements because they were found to contain an undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
July 01, 2013
Teas Recalled Due To Potential Botulism Contamination
One June 28, 2013, Harmony Chai issued a voluntary recall of its Concentrated Black Spiced Chai and Decaffeinated Rooibos Chai bottled tea drinks, because they have the potential to be contaminated with Clostridium botulinum.
Recalls & Warnings
March 19, 2019
FDA Calls Promotion of Nyloxin Homeopathic Products for Pain a "Health Fraud Scam"
On March 11, 2019, the FDA issued a warning letter to Nutra Pharma Corp. following a review of the company's website (www.Nyloxin.com) and social media sites found that the company was making drug claims about its homeopathic products promoted for arthritis and cancer pain.
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
September 01, 2018
Homeopathic Remedies Contaminated With Bacteria
On August 29, 2018, Hellolife, Inc.
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
March 11, 2003
Rexall Agrees to Pay up to $12 million to Users of Misleading Cellulite Supplement
On March 11, 2003, the Federal Trade Commission (FTC) reported that Rexall Sundown, Inc. (Rexall) will pay up to $12 million to resolve FTC charges regarding its marketing of the dietary supplement, "Cellasene," a purported cellulite treatment product.
Recalls & Warnings
June 23, 2017
FDA Warns Seller of Menopause, Sexual Enhancement, Prostate Supplements and More For Manufacturing Violations
On May 26, 2017 the FDA issued a warning letter to Star Health & Beauty LLC, following a facility inspection which found the company's products, including Nu Essentials Royal Jelly Capsules, NuMan Male Enhancement Capsules, Star's Male Potency Tonic, NuGen HP, She Max HP, and V Max ...
Recalls & Warnings
April 04, 2013
Three More Sexual Enhancement Supplements Found To Contain Undeclared Drugs
On April 3, 2013, the FDA warned consumers that the sexual enhancement supplements AFFIRM XL, Love Rider and Ninja Mojo were found to contain undeclared erectile dysfunction drugs. Consumers are urged to stop using these supplements immediately.
Recalls & Warnings
May 30, 2015
Seller of Omega-3, Probiotics & SuperFoods Warned for Manufacturing Violations, Drug Claims
On May 4, 2015, the FDA issued a warning letter to Dr. Dennis Black, LLC.
Recalls & Warnings
January 30, 2014
Five Sexual Enhancement Supplements Found to Contain Prescription Drugs
On January 28, 2014, the FDA warned consumers not to buy or use the five sexual enhancement supplements listed below because they were found to contain sildenafil and/or tadalafil.
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
November 06, 2014
Seller of Cholesterol, Arthritis Supplements and More Warned for Drug Claims
On October 17, 2014, the FDA issued a warning letter to Vitamins Direct (USA) and Golden Pride, Inc., which distribute Flexezy and Physician's Signature brands of dietary supplements, following a facility inspection which found statements made about certain supplements to be drug claims.
Recalls & Warnings
July 25, 2013
Beware of Dietary Supplements With Claims To Treat Diabetes, FDA Warns
On July 23, 2013, the FDA issued a warning to consumers not to buy or use dietary supplements that are promoted to treat diabetes.
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.
