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RECALL RECORD — CLASS IRecall closedF-0080-2023/FDA enforcement
Best Nutritionals LLC·Dietary Supplements·Aug 29, 2022

White Plastic Bottle with Green, Gold, and Blue Labeling Containing 360, 610mg Hard Gelatin…

What you need to know

Class I

  • What happened

    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…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameBest Nutritionals LLC
Recalling firmBest Nutritionals LLCPiscataway, NJ, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Best By 10/24 Lot 102120
Distribution area

The product was distributed thru the internet, via customers through FBA & WFS.

United States

Quantity affected3580 Bottles
Recall initiationFDA report date: October 26, 2022
FDA recall numberF-0080-2023

Beyond the headline

The recall, in context

Best Nutritionals LLC initiated this supplements recall on August 29, 2022. The FDA enforcement report states: 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. The FDA report lists distribution as: The product was distributed thru the internet, via customers through FBA & WFS.

The FDA enforcement report describes the reason as: 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.

White Plastic Bottle with Green, Gold, and Blue Labeling Containing 360, 610mg Hard Gelatin… was made or distributed by Best Nutritionals LLC in Piscataway, NJ, United States. This page reflects FDA report F-0080-2023, dated October 26, 2022.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a bacteria commonly linked to poultry, eggs, sprouts and seeded vegetables. Infection can cause fever, cramps and diarrhea.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Salmonella

Symptoms to watch for

Diarrhea, fever, abdominal cramps, nausea and sometimes vomiting. Symptoms can be severe in young children, older adults and immunocompromised people.

When symptoms may appear

Usually 6 hours to 6 days after exposure; illness often lasts 4 to 7 days.

Higher-risk groups

Children under 5, adults over 65, pregnant people and anyone with a weakened immune system are more likely to develop severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the White Plastic Bottle with Green, Gold, and Blue Labeling Containing 360, 610mg Hard Gelatin… recall?

Best Nutritionals LLC recalled White Plastic Bottle with Green, Gold, and Blue Labeling Containing 360, 610mg Hard Gelatin… in an FDA Class I enforcement action reported as F-0080-2023. 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…

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Best Nutritionals LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0080-2023. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.