White plastic bottle with green recall
Recalled by Best Nutritionals LLC · Piscataway, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it 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.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
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
Quantity: 3580 Bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Best By 10/24 Lot 102120
Where it was sold
FDA's distribution note: The product was distributed thru the internet, via customers through FBA & WFS.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Best Nutritionals LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 29, 2022
- In FDA report of
- Oct 26, 2022
- Terminated
- Jan 13, 2023
- FDA recall number
- F-0080-2023 · event 90815
- Official record
- FDA enforcement report search