Wellements LLC of Scottsdale, Arizona is voluntarily recalling Wellements Iron Drops liquid dietary supplement and the sample version called Iron Drops Sample liquid Dietary Supplement because they may contain milk, one of the major food allergens, that is not printed on the label. Anyone who is allergic to milk or who is lactose intolerance could have a serious allergic reaction if they eat this product. One allergic reaction has been reported to the company. The recalled Wellements Iron Drops were distributed from May 1, 2019 to July 22, 2020 nationwide through retail stores, Amazon, and Wellements.com. The sample was also distributed during that time frame through promotional giveaways in some consumer purchases. This product is used in infants 4 months of age to children up to … [Read more...]
UpSpring Baby Iron Is Being Recalled For Undeclared Milk
UpSpring LLC of Austin, Texas is recalling one batch of UpSpring Baby Iron + Immunity dietary supplement because it may contain milk, one of the major food allergens, that is not declared on the label. Any child with a milk allergy or lactose intolerance could have a serious reaction if they consume this product. No allergic reactions have been received by the company to date in connection with this issue. The recalled product is UpSpring Baby Iron + Immunity that is sold in 60 ml dark brown glass bottles. The lot number is 06691 and the expiration date is March 2021. The lot number and expiration dates are on the bottom of the carton printed in black ink, and the bottom of the glass bottle, printed in yellow ink. This product was distributed nationwide via online sales through … [Read more...]
Sundial Herbal Products Recalled For Unapproved Drugs and Misbranding
Sundial Herbal Products are being recalled for unapproved drugs to be in compliance with FDA Drug Regulations. These recalled products are misbranded because they have labeling claims that could result in delay of appropriate treatment by a healthcare provider. Because these dietary supplements are unapproved, their safety and efficacy have not been established. No illnesses or adverse reactions have been reported by the company to date. The recall headline states that "recall is required by the order." All products used as Sundial Herbs can be identified with the "Sundial" label. They were sold in brown glass bottles, boxes, ziplock bags, and paper bags wit clear viewing windows. They were distributed nationwide or statewide through the Sundial Herb website or any other website. … [Read more...]
Mountain Rose Herbs Kudzu Root Recalled For Possible Salmonella
Mountain Rose Herbs Kudzu Root Herbal Supplement is being recalled because it may be contaminated with Salmonella. No illnesses have been reported to date in connection with this issue. The recalled product is Organic Kudzu Root Herbal Supplement with lot numbers 24247-X and 24247. It was sold to customers who ordered from the company's website and was also sold at the company's retail shop in Eugene, Oregon. And it was sold through mail orders by phone or fax from June 17, 2019 to March 2, 2020. In addition, the product may have been resold. Mountain Rose Herbs Kudzu Root was also distributed directly to customers in Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Massachusetts, Maryland, … [Read more...]
ReStructure Vanilla Protein Powder Recalled For Undeclared Milk
New Capstone, Inc. of Mooresville, North Carolina is recalling their ReStructure Vanilla Protein Powder pouches in specific sizes and lot numbers because they may contain milk, one of the major food allergens, that is not printed on the label. Anyone who is lactose intolerant or who is allergic to milk could have a serious reaction or illness if they eat this product. No illnesses or allergic reactions have been reported to the company to date. The products were distributed through New Capstone's website from October 21, 2019 through January 8, 2020. The powder was shipped nationwide directly to consumers via an eCommerce website. The recalled product is ReStructure Vanilla Protein Powder pouches in 22 ounce size. The lot number is 19211 and the expiration date is 06/21. Also … [Read more...]
Recall of Nopalina Flax Seed Products For Salmonella Updated
The recall of Nopalina Flax Seed products for possible Salmonella contamination has been updated with new information. The new info includes lot numbers that were not previously listed in the January 28, 2020 announcement. No illnesses have been reported to date in connection with this recall issue. The FDA first issued a public health alert about this problem, then the company recalled their products. Lot numbers are on the bottom back of the product package. The lot numbers that are on the recalled products are: The following lot numbers are affected by this recall (the lot numbers can be found on the bottom back of Nopalina Flax Seed Fiber (powder, 1 lb. bags) UPC 890523000720 Lot # 62.19 / 1 # 52.1 Best if used by 10/7/21 Lot # 62.19 / 2 # 52.1 Best if used by … [Read more...]
FDA Issues Health Alert Over Nopalina Flax Seed For Salmonella
The FDA has issued a public health alert about Nopalina Flax Seed Powder and Nopalina Flax Seed Capsules for possible Salmonella contamination. These products were manufactured by Salud Natural Entrepreneur, Inc. The recalled products include: Nopalina Flax Seed Fiber (powder, 1 lb. bags) Lot # 62.19/9#52.1 Best if used by 10/7/21 Lot # 62.19/2#52.1 Best if used by 10/7/21 Nopalina Flax Seed Fiber (powder, 1 lb. bags) Lot # 64.19/3#52.1 Best if used by 10/21/21 Nopalina Flax Seed Fiber (powder, 2 lb. bags) Lot # 64.19/2#52.1 Best if used by 10/21/21 Lot # 64.19/2*2Lb#52.1 Best if used by 10/21/21 Nopalina Flax Seed Fiber (powder, 1 lb. bags) Lot # 65.19/1#52.1 Best if used by 10/24/21 Lot # 65.19/2#52.1 Best if used by 10/24/21 Nopalina Flax … [Read more...]
Dietary Supplement Manufacturer ABH Pharma Recalls All Products
According to the FDA, ABH NATURE’S PRODUCTS, INC, ABH PHARMA, INC., and STOCKNUTRA.COM, INC. (the “COMPANIES”) is recalling all lots of its dietary supplements sold nationwide because of a Consent Decree entered by the U.S. District Court for the Eastern District of New York. All of the company's products that were manufactured and sold between January 2013 through November 2019 are recalled. The FDA found "significant violations of current good manufacturing practice regulations" after an inspection. This problem represents the risk of supplements that have "decreased identity, purity, strength, and composition," according to the notice. No illnesses, injuries, or adverse reactions have been reported to date in connection with this problem. These companies, ABH NATURE’S … [Read more...]
Cellect Products Recalls Unflavored Powder For Arsenic and Lead
Port Jefferson Station, NY, Cellect Products Inc. and Oglethorpe Ltd. are recalling lot #041907 of Cellect Unflavored Powder & Essentials Factor Cell Synergy Unflavored Powder. because they have unsafe levels of arsenic and lead. Long term exposure to inorganic arsenic is associated with skin disorders and increased risks for skin, bladder, and lung cancers. Long term exposure to lead can cause learning disabilities and lower IQ. No reports of adverse reactions have been received to date. Taking more than two servings daily of this drink mix product could result in an accumulation of lead in the body. Lead poisoning can damage the nervous system and internal organs. Acute lead poisoning can cause abdominal pain, nausea, vomiting, muscle weakness, diarrhea, weight loss, and bloody or … [Read more...]
Mero Macho Passion Fruit Vitamin C Supplement Recalled For Tadalafil
Fitoterapia USA is recalling 19,000 bottles of Mero Macho Passion Fruit Flavored Vitamin C Liquid Supplement because it is tainted with Tadalafil, the active ingredient in an FDA-approved drug that is used for the treatment of male erectile dysfunction. That makes the product an unapproved drug for which safety and efficacy have not been established. Anyone who takes dietary supplements could have underlying diseases such as hypertension, diabetes, or high cholesterol. And these patients often take nitrates. Use of nitrates and phosphodiesterase 5-inhibits can lead to "fatal cardiovascular collapse," according to the recall notice. There have not been any reports of adverse reactions related to this recalled product. The product is marketed as a dietary supplement and is packaged in … [Read more...]
