Nutreglo Blood & Internal Cleanser Recall: Drug Claims and Iron Issues
Nutreglo Products recalls Blood & Internal Cleanser dietary supplement due to undeclared drug claims and incorrect iron content. Check your expiration date.
Use caution until it’s fixed
The product Blood & Internal Cleanser is a dietary supplement with drug claims and iron content at 67 & 69% of declared, per laboratory results. The product Belly Fat Reducer + Energy Booster and Stamina declares incorrect amount of Vitamin B6. The product label declares 50mg and only contains 0.1 mg as per laboratory results.
Contact the company
What happened, in plain English
Nutreglo Products, LLC is recalling its Blood & Internal Cleanser dietary supplement because laboratory results showed it contained undeclared drug claims and had iron levels that were 67% to 69% of what was declared on the label. The recall also covers other products like Belly Fat Reducer + Energy Booster for incorrect Vitamin B6 amounts, but this summary focuses on the Blood & Internal Cleanser. Consumers should be aware that the supplement does not match its label specifications. Read more at govinfonow.com/recall/19111-nutreglo-blood-internal-cleanser-recall-drug-claims-and-iron-issues.
Source Summary by GovInfoNow · govinfonow.com/recall/19111-nutreglo-blood-internal-cleanser-recall-drug-claims-and-iron-issues · Updated October 11, 2026 · FDA enforcement record: FDA #F-1591-2018
Cite this page
“Nutreglo Blood & Internal Cleanser Recall: Drug Claims and Iron Issues.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19111-nutreglo-blood-internal-cleanser-recall-drug-claims-and-iron-issues. Based on FDA recall #F-1591-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1591-2018%22&limit=1).
Why it’s dangerous
The primary danger is that the product contains undeclared drug claims, which means it may contain active pharmaceutical ingredients not listed on the label, posing unknown health risks. Additionally, the iron content was found to be significantly lower than declared (67-69% of stated amount), meaning users relying on it for iron supplementation are not getting the intended dosage.
Who’s affected
Consumers in the United States who purchased Nutreglo Products' Blood & Internal Cleanser dietary supplement are affected by this recall. Individuals relying on the product for specific iron intake or expecting it to function as a standard dietary supplement without undeclared ingredients are most at risk.
How to tell if you have this one
Look for the product name 'Blood & Internal Cleanser, Dietary Supplement' manufactured by Nutreglo Products, LLC. The specific batch mentioned has an expiration date of 12-2020. The distribution was limited to U.S. consignees only.
- Brand
Nutreglo Products- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Status
Terminated- Distribution
US consignees only.
| Recall number | Product, codes & lots | Quantity | Class |
|---|---|---|---|
| F-1590-2018 | Belly Fat Reducer + Energy Booster and Stamina, Dietary Supplement; Batch #125 for Belly Fat Reducer and Batch # 134 for Blood & Internal Cleanser. Both with Expiration Date of 12-2020 | 48 packages (16 each) for Belly Fat Reducer and 60 packages (16 each) | Class III |
| F-1591-2018 | Blood & Internal Cleanser, Dietary Supplement; Expiration Date 12-2020 | 60 packages (16 each) for Blood & Internal Cleanser | Class II |
What to do — step by step
Stop using the product
Discontinue use of the Blood & Internal Cleanser dietary supplement immediately due to label inaccuracies and undeclared drug claims.
Check expiration date
Verify if your package has an expiration date of 12-2020 to confirm it is part of the recalled lot.
How this recall unfolded
Recall timeline
FDA terminated this recall 16 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1591-2018 (May 20, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1591-2018 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.