Recall record at a glance
| Official record | F-1590-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Nutreglo Products, LLC. |
| Report date | Jul 4, 2018 |
| Recall initiation date | May 20, 2018 |
| Quantity | 48 packages (16 each) for Belly Fat Reducer and 60 packages (16 each) |
| Location | Fort Lauderdale, FL, United States |
Official product description
Belly Fat Reducer + Energy Booster and Stamina, Dietary Supplement
Why the product was recalled
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.
Distribution information
US consignees only.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Telephone.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.