Hi-Tech Pharmaceuticals of Norcross, Georgia is recalling all lots of APS Nutrition Isomorph dietary supplement flavors in different size jugs because they contain milk, wheat, and soy, three of the major food allergens, that are not declared on the label. All lots of iForce Nutrition Mass Gainz Brown Sugar Maple Oatmeal Cookie in 4.85 pound jugs and 10 pound bags is recalled because it contains undeclared eggs. Anyone who is allergic to milk, wheat, eggs, or soy, or who is lactose intolerant or who has celiac disease, could have a serious reaction if they eat these products. No illnesses or allergic reactions have been reported to the company to date in connection with the consumption of these items. You can see the long list of recalled products, along with package sizes, UPC … [Read more...]
Some Isagenix Products Recalled in Canada For Overfortification of Vitamins Being Sold on Internet Sites
Certain Isagenix International products recalled in Canada last year because of over-fortification of vitamins are currently being sold through various Internet sites that are not affiliated with Isagenix, according to the Canadian Food Inspection Agency. There have been illnesses reported to the company and the Canadian government due to the consumption of these products, which were recalled on Oct. 31, 2020, Nov. 7, 2020, and Nov. 14, 2020. You can see the long list of recalled products at the CFIA web site, along with the package size, UPC numbers, and codes on the products. Some of the recalled products are Isalean Bars, including the flavors Chocolate Cream Crisp and Chocolate Peanut Crunch; and Isalean Shakes, including the flavors Creamy Dutch Chocolate, Birthday Cake Flavor, … [Read more...]
Wellements Iron Drops Are Being Recalled For Undeclared Milk
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...]
