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Recalls & Warnings
November 12, 2025
Organic Moringa Leaf Powder Recalled Due to Salmonella
On November 6, 2025, Africa Imports recalled its Organic Moringa Leaf Powder after some of the Moringa powder tested positive for Salmonella.
News Release
August 01, 2006
ConsumerLab.com evaluates cholesterol-lowering supplements — Test results available for over 90 products; Review of nine popular ingredients
WHITE PLAINS, NY — AUGUST 1, 2006 — ConsumerLab.com has released a major new review of dietary supplements used to improve cholesterol and triglyceride levels.
Recalls & Warnings
November 17, 2025
Food to Live Organic Moringa Leaf and Supergreens Mix Recalled
On November 12, 2025, Food To Live recalled its Organic Moringa Leaf Powder and Organic Supergreens Powder Mix after a supplier lot of organic moringa powder tested positive for Salmonella.
Recalls & Warnings
January 15, 2024
Suprex Carb & Sugar Block Recalled
On December 7, 2023, Vita 360, LLC issued a recall of one lot of SUPREX Plant Based Nutrition Carb & Sugar Block after FDA analysis found it to contain only 16 mcg of chromium per serving and not 100 mcg of chromium per serving, as listed on the label.
Recalls & Warnings
January 28, 2021
FDA Issues Import Alert on Potentially-Dangerous Hand Sanitizers from Mexico
On January 26, 2021, the FDA announced that all alcohol-based hand sanitizers from Mexico will be placed on a countrywide import alert to limit the flow of potentially dangerous products into the US.
Recalls & Warnings
July 28, 2022
FDA Warns Three Manufacturers of Sanitizer for Manufacturing and Misbranding Violations
Between July 8 and July 21, the FDA issued warning letters to three companies selling hand sanitizer products that violate Current Good Manufacturing Practices (cGMP), are adulterated and misbranded, and for refusal to allow the agency to access and copy company records.
Recalls & Warnings
February 09, 2021
Three More Hand Sanitizers Contain Toxic Ingredient
Between February 3 and 5, 2021, the FDA issued warning letters to three sellers of hand sanitizers because laboratory tests showed that their products contain methanol, which is toxic when absorbed through the skin or ingested.
Recalls & Warnings
April 27, 2022
FDA Tests Find Imported Hand Sanitizer Contains Less Active Ingredient Than Claimed
On April 19th, 2022, the FDA issued a warning letter to Guangzhou Zhongkebaishi Health Industry Co., Ltd.
Recalls & Warnings
August 07, 2021
Poppy Seed Tea, Unwashed Poppy Seeds Pose Risk of Overdose, Death
Unwashed poppy seeds can be contaminated with significant, even dangerous levels of opioid compounds that can cause serious adverse effects, overdose and death.
Recalls & Warnings
February 09, 2021
FDA Warns Two Sellers of Adulterated Hand Sanitizers
Between January 28 and February 3, 2021, the FDA issued warning letters to two sellers of hand sanitizers because laboratory tests showed that their products do not contain the amount of ethanol as stated on their labels.
Recalls & Warnings
January 17, 2006
FDA Warns Consumers about Brazilian Diet Pills Found to Contain Active Drug Ingredients
On January 13,2006, the U.S. Food and Drug Administration (FDA) warned consumers not to use two unapproved drug products that are being marketed as dietary supplements for weight loss.
Recalls & Warnings
September 09, 2011
Possible Concern with Fenugreek Based on Contamination in Europe
Products made with fenugreek, including pills containing fenugreek seed, have been pulled from shelves in Germany due to conern over potential contamination with E. coli bacteria. There is no such action in the U.S., but ConsumerLab.
Recalls & Warnings
October 21, 2015
Imported Supplements Can Be Dangerous, FDA Warns
On October 15, 2015, the FDA warned consumers that some supplements sold at nontraditional places, such as ethnic or international stores, flea markets, swap meets, as well as online, are often imported from other countries, and some can potentially be harmful.
Recalls & Warnings
February 17, 2018
FDA Reports Prevalence of Salmonella In Retail Spices
An FDA study of 11 different types of spices sold in retail stores throughout the U.S. found the prevalence of Salmonella contamination to be less than 1%. Overall, this was significantly lower than when the same types of spices were tested at the time of import to the U.S.
Recalls & Warnings
September 02, 2016
Kratom To Be Classified a Schedule I Controlled Substance
On August 30, 2016, the U.S. Drug Enforcement Agency (DEA) announced its intent to classify the active compounds (mitragynine and 7-hydroxymitragynine) in kratom as Schedule I controlled substances.
Recalls & Warnings
August 05, 2016
U.S. Marshals Seize $150,00 Worth of Kratom
On August 4, 2016, the FDA announced that U.S. Marshals seized approximately $150,000 worth of dietary supplements labeled as containing kratom from Nature Therapeutics (dba Kratum Therapy). The action was taken at the request of the FDA.
Recalls & Warnings
January 12, 2016
Over $400,000 Worth of Kratom Supplements Seized by U.S. Marshals
On January 6, 2016, U.S. Marshals seized nearly 90,000 bottles of dietary supplements labeled as containing kratom (brand name RelaKzpro) valued at over $400,000, from Dordoniz Natural Products LLC in South Beloit, Illinois. The action was taken at the request of the FDA.
Recalls & Warnings
September 30, 2014
U.S. Marshals Seize $5 Million Worth of Kratom
On September 25, 2014, U.S. Marshals seized more than 25,000 pounds of raw kratom valued at over $5 million from Rosefield Management, Inc. in Van Nuys, California. The action was taken at the request of the FDA.
Recalls & Warnings
March 21, 2014
Products Containing Kratom Recalled Following FDA Import Alert
On March 14, 2014, SNI National issued a voluntary recall of all kratom supplements, including kratom XL 4 Pack, Maeng Da Kratom 10 Pack, Max Kratom 20 Pack, and Bali Kratom 40 pack, following an FDA-issued import alert on all products containing this ingredient.
Recalls & Warnings
November 28, 2015
FDA Warns Consumers Not to Buy or Use "Sex Drive Capsules"
On November 19, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Sex Drive Capsules because they were found to contain sildenafil.
Recalls & Warnings
November 07, 2015
Power Khan Herbal Enhancement Supplement Found to Contain Drug
On November 5, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Power Khan because it was found to contain sildenafil.
Recalls & Warnings
October 24, 2015
Drug Found in Male Enhancement Supplement
On October 23, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement S.W.A.G.G.E.R Extreme because it was found to contain sildenafil.
Recalls & Warnings
May 17, 2016
Sexual Enhancement Supplement Contains Undeclared Drugs
On May 6, 2016, the FDA issued a warning letter to Economax, LLC because the company's sexual enhancement supplement, Super Power Khan was found to contain sildenafil and hydroxyhomosildenafil.
Recalls & Warnings
August 31, 2012
Recent Cases of Lead Poisoning From Ayurvedic Medications from India
Public health officials have reported six cases of lead poisoning among foreign-born women who took Ayurvedic herbal products imported from India. The cases were reported by the New York City Department of Health and Mental Hygiene.
Recalls & Warnings
September 17, 2003
FDA Warns of Illness from Star Anise Teas
On September 10, 2003, the Food and Drug Administration (FDA) advised consumers not to consume "teas" brewed from star anise.
Recalls & Warnings
August 15, 2002
FDA Warns Public About Chinese Diet Pills Containing Fenfluramine
On August 13, the U.S. FDA alerted the public about Chinese weight-loss products, Chaso (Jianfei) Diet Capsules and Chaso Genpi, because they pose a potential public health risk.
Recalls & Warnings
June 20, 2002
Canadian Warning on Use of Bejai Bowyantan for Infants
On June 14, 2002, Health Canada warned Canadians not to use Bejai Bowyantan for their young children and infants because it contains a substance with similar toxic properties to another substance known to cause serious adverse reactions and death in children.
Recalls & Warnings
September 13, 2010
ExtenZe Enhancement Supplements Seized in Canada
On August 19, 2010, Health Canada (Canada's health ministry) seized the sexual enhancement supplements "Male Enhancement ExtenZe" and "Women ExtenZe" which were imported from the U.S. Although legal and widely sold in the U.S.
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
November 03, 2004
FDA Warns of Sexual Enhancement Supplements Containing Prescription Drug
On November 2, 2004, the Food and Drug Administration (FDA)warned consumers not to purchase or to consume Actra-Rx or Yilishen, two products promoted and offered for sale on Web sites as "dietary supplements" for treating erectile dysfunction and enhancing sexual performance for men.
Recalls & Warnings
May 15, 2016
Sexual Enhancement Supplements Recalled
On May 10, 2016, SOS Telecom, Inc. issued a recall of the following sexual enhancement supplements, which were found to contain undeclared sildenafil:
Recalls & Warnings
March 20, 2016
Salute Capsules Contain Hidden Drugs
On March 17, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Salute Capsules because it was found to contain sildenafil, thiosildenafil, and sulfoaildenafil.
Recalls & Warnings
March 04, 2016
FDA Warns Consumers Not To Use Sexual Enhancement Supplement
On March 3, 2015, the FDA warned consumers not to buy or use the sexual enhancement supplement Sextra because it was found to contain sildenafil.
Recalls & Warnings
February 27, 2016
Enhancement Supplement Contains Undeclared Drug
The FDA recently warned consumers not to buy or use the sexual enhancement supplement Neophase Natural Sex Enhancer because it was found to contain hydroxyacetildenafil.
Recalls & Warnings
January 22, 2016
Male Enhancement Gum and Pills Contain Hidden Drug
On January 21, 2016, the FDA warned consumers not to buy or use the following sexual enhancement supplements, because they were found to contain undeclared vardenafil (click on the name of each supplement to read the FDA's complete warning):
Recalls & Warnings
January 21, 2016
Morphine Found in Licorice Product
On January 20, 2016, Master Herbs, Inc. issued a recall of all lots of Licorice Coughing Liquid because it was found to contain morphine.
Recalls & Warnings
February 06, 2018
FDA Links 44 Deaths to Kratom
On February 6, 2018, FDA announced it is now aware of 44 deaths associated with the use of kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms. This is an increase from the 36 deaths associated with kratom that the agency reported in November 2017.
Recalls & Warnings
November 14, 2017
36 Deaths Associated With the Use of Kratom Products
On November 14, 2017, FDA Commissioner Scott Gottlieb, M.D. issued a statement on the dangers of using products containing kratom, an herb often promoted for pain relief, energy and for treating opioid withdrawal symptoms.
Recalls & Warnings
May 26, 2017
Herbal "Sexual Enhancement Coffee" Recalled, One Death Reported
On May 25, 2017, Caverflo.com issued a recall of Caverflo Natural Herbal Coffee, an "herbal" instant coffee promoted for sexual enhancement, because it was found to contain the drugs sildenafil and tadalafil.
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
April 19, 2017
Sexual Enhancement Supplements for Men and Women Recalled
On April 18, 2017, Organic Herbal Supply, Inc. issued a recall of all lots of the following sexual enhancement supplements for men because they were found to contain the undeclared drug tadalafil:
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
March 04, 2017
Sexual Enhancement Supplements Found to Contain Drugs
On March 3, 2017, the FDA warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared drugs:
Recalls & Warnings
February 21, 2017
Sexual Enhancement Supplement Recalled
On February 16, 2017, Organic Herbal Supply, Inc. issued a recall of its sexual enhancement supplement XtraHRD Natural Male Enhancement because it was found to contain tadalafil.
Recalls & Warnings
February 04, 2017
FDA Warns Four Sexual Enhancement Supplements Contain Prescription Drug
The FDA recently warned consumers not to buy or use the following sexual enhancement supplements because they were found to contain undeclared sildenafil.
Recalls & Warnings
December 29, 2016
Sexual Enhancement Supplement Contains Prescription Drug
On December 22, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Power Male Sexual Stimulant because it was found to contain sildenafil. This supplement was identified during an examination of international mail shipments.
Recalls & Warnings
December 23, 2016
Twelve Sexual Enhancement Supplements Found to Contain Prescription Drug
On December 22, 2016, the FDA warned consumers not to buy or use the following twelve sexual enhancement supplements because they were found to contain undeclared sildenafil. Each was identified during an examination of international mail shipments.
Recalls & Warnings
December 03, 2016
Male Enhancement Supplement Recalled
On November 29, 2016, MS Bionic, Inc. issued a recall of all lots of Megajex Natural Male Sex Enhancer capsules because they were found to contain tadalafil and sildenafil.
Recalls & Warnings
November 11, 2016
Male Enhancement Supplement Contains Hidden Drug
On November 9, 2016, the FDA warned consumers not to buy or use the sexual enhancement supplement Ready Man! because it was found to contain sildenafil and phenolphthalein.
Recalls & Warnings
October 24, 2015
Eight Enhancement Supplements Found to Contain Undeclared Drugs
On October 23, 2015, the FDA warned consumers not to buy or use the following three sexual enhancement supplements because they were found to contain an undeclared sildenafil or similar drugs (some were identified during an examination of international mail shipments):
Recalls & Warnings
October 12, 2013
Metagenics Enzyme Supplement Recalled Due To Drug Risk
On October 11, 2013, Metagenics Canada issued a voluntary recall of digestive enzyme supplement Spectrazyme, due to potential contamination with the prescription antibiotic chloramphenicol.
Recalls & Warnings
December 19, 2015
"Tiger X" and "X Again Platinum" Contain Hidden Drugs
On December 17 and 18, 2015, the FDA warned consumers not to buy or use the following sexual enhancement supplements, which were found to contain undeclared drugs:
Recalls & Warnings
December 01, 2015
Enhancement Supplements Found to Contain Prescription Drug
On November 19, 2015, the FDA warned consumers not to buy or use the following sexual enhancement supplements, which were identified during an examination of international mail shipments, because they were found to contain undeclared sildenafil (click on the name of each supplement to read the ...
Recalls & Warnings
April 12, 2019
Sexual Enhancement Supplement for Men Recalled
On April 9, 2019, SD Import, LLC issued a recall of Aphrodisiac, a supplement promoted for male sexual enhancement, because FDA analysis found it to contain sildenafil.
Recalls & Warnings
November 27, 2018
High Levels of Lead Found in Kratom Products
Some kratom products contain levels of lead and nickel that are not considered safe for human consumption, according to tests conducted by the FDA.
Recalls & Warnings
May 29, 2018
FDA Warns Seller of "Aromatase Inhibitor" Supplement
On May 18, 2018, the FDA issued a warning letter to Performance Nutrition Formulators LLC d.b.a. VMI Sports because its product Arimistane contains Androsta-3,5-Diene-7,17-Dione, an ingredient that the FDA considers to be a new drug and not a dietary supplement ingredient.
