FDA Recalls Nutreglo Blood & Internal Cleanser for Incorrect Iron Content
Nutreglo Products, LLC. is recalling Blood & Internal Cleanser dietary supplements because laboratory results showed incorrect iron levels and drug claims.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a situation that could cause temporary or medically reversible adverse health consequences. The primary issues are mislabeling of iron content and drug claims, which align with moderate severity criteria for labeling errors and low-risk contamination.
Plain-English summary
Nutreglo Products, LLC. is voluntarily recalling Blood & Internal Cleanser, a dietary supplement. The recall was initiated because laboratory results indicated that the product contains iron at 67% and 69% of the declared amount. Additionally, the product was found to make drug claims.
The recall involves 60 packages (16 each) of Blood & Internal Cleanser with an expiration date of 12-2020. The source text also notes that a related product, Belly Fat Reducer + Energy Booster and Stamina, declares an incorrect amount of Vitamin B6, stating 50mg on the label but containing only 0.1 mg.
Consumers who have purchased these products should stop using them and contact the recalling firm for further instructions. The distribution was limited to US consignees.
The recalled product
- Product
- Blood & Internal Cleanser, Dietary Supplement
- Manufacturer
- Nutreglo Products, LLC.
- Category
- Food — Dietary Supplement
- Hazard
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 (1)
- Expiration Date 12-2020
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 2 recalled by Nutreglo Products, LLC. 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.
See all 2 products in this recall →Related recalls
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