NutriLean Dietary Supplement Contains Undeclared Food Dyes
Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplements nationwide because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes, which are not listed on the label.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: This is an FDA Class III recall involving undeclared food dyes in gelatin capsules. The hazard is labeling-related and does not involve known foodborne pathogens, allergen mislabeling of major allergens, or reported illnesses. Class III recalls are by definition unlikely to cause adverse health consequences.
Plain-English summary
Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplement capsules distributed nationwide in the United States. The product's gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1), which are not declared on the product label. The affected lot codes are 21745-11, 21745-12, 21745-13, 21745-14, and 21745-15.
Consumers who have purchased this product should stop using it. Individuals concerned about potential adverse reactions should consult their healthcare provider. The product does not have a UPC code. For more information, consumers may contact Preventics, Inc. dba Legere Pharmaceuticals at the address listed: 15344 N 83rd Way, Scottsdale, AZ 85260.
The recalled product
- Product
- NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
- Manufacturer
- Preventics, Inc. dba Legere Pharmaceuticals
- Category
- Drug — Dietary Supplement
- Affected units
- 94,190
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- 21745-11
- 21745-12
- 21745-13
- 21745-14
- 21745-15
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 6 recalled by Preventics, Inc. dba Legere Pharmaceuticals under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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