Recall record at a glance
| Official record | F-0080-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | BEST NUTRITIONALS LLC |
| Report date | Oct 26, 2022 |
| Recall initiation date | Aug 29, 2022 |
| Quantity | 3580 Bottles |
| Location | Piscataway, NJ, United States |
Official product description
White plastic bottle with green, gold, and blue labeling containing 360, 610mg hard gelatin capsules of Fenugreek seed powder, labeled in part, "Best Naturals Fenugreek Premium Herbal 610mg 3rd Party Lab Tested 360 CAPSULES DIETARY SUPPLEMENT", best by 10/24, lot 102120
Why the product was recalled
Best Nutritionals LLC 120 Centennial Ave, Piscataway NJ 08854, is initiating a recall of Fenugreek 610 mg , 360 Capsules ,in White Plastic HDPE bottles because the product has the potential to be contaminated with Salmonella.
Distribution information
The product was distributed thru the internet, via customers through FBA & WFS.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly 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.