70 FDA warnings on file. View details
Scores across 3 products from this brand, from lowest to highest:
Product recalled due to undeclared niacin.
Glass fragments.
Product recalled because of the presence of mold and/or yeast found in amounts that exceed the product's established specifications .
Label declares lecithin but does not declare soy lecithin.
Label declares lecithin but does not declare soy lecithin.
Label declares lecithin but does not declare soy lecithin.
The firm is recalling their products due the unapproved use of a food additive and unapproved marketing statements
All scores are algorithmically generated from publicly available label data (NIH Dietary Supplement Label Database) and reflect label quality — dosage transparency, ingredient disclosure, and formula cleanliness — not clinical efficacy, safety, or product quality. This page is not affiliated with or endorsed by EA. If you represent this brand and believe any information is inaccurate, please contact us for a correction. Read full methodology
Due to different color of powder in capsules. Firm's evaluation determined product low potency.
Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).
Undeclared allergens: soy (lecithin)
Undeclared allergens: soy (lecithin)
Undeclared allergens: soy (lecithin)
Undeclared allergens: milk (Colostrum)
Undeclared allergens: soy (lecithin)
Undeclared allergens: milk (Whey)
Undeclared allergens: soy (lecithin)
The product is being recalled due to the potential presence of Salmonella.
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Protein supplement fails to declare allergen milk
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergen milk
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergens: milk, shellfish
Protein supplement fails to declare allergens: milk and coconut
Protein supplement fails to declare allergens: milk
Protein supplement fails to declare allergen milk
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergen milk
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergens: milk, shellfish
Protein supplement fails to declare allergens: milk
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergens: milk, shellfish
Protein supplement fails to declare allergen: milk
Protein supplement fails to declare allergen milk
Protein supplement fails to declare allergens: milk
Protein supplement fails to declare allergens milk
Protein supplement fails to declare allergens: milk, shellfish
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
Product recalled due to undeclared niacin.
Label declares lecithin but does not declare soy lecithin.
Sublinqual B12 tablets are recalled because the ingredients statement declared lactose but label does not declare milk.
Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules is being recalled because a material review was conducted in April 2015. It revealed some of the Chondroitin Sulfate (Lot 093011 1031) raw material used in the manufacture of Maxiflex Multinutrient Formula Lot 32171215 was Out of Specification.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.