RECALL RECORD — CLASS IRecall closedF-0996-2018/FDA enforcement

Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.s.a

What you need to know

Class I
  • What happened

    Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.

  • 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 FDAIN, UTMore supplements

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Match before you discard

Product identification

Source: FDA FOOD

Brand nameAvalon Packaging
Recalling firmAvalon PackagingOrem, UT, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot 171409
Distribution area
INUT

Sold to Label owner in UT.

United States

Quantity affected1108 bottles
Recall initiationFDA report date: March 28, 2018
FDA recall numberF-0996-2018

Beyond the headline

The recall, in context

Avalon Packaging initiated this supplements recall on March 9, 2018. The FDA enforcement report states: Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination. The FDA report lists distribution as: Sold to Label owner in UT.

The FDA enforcement report describes the reason as: Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.

Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.s.a was made or distributed by Avalon Packaging in Orem, UT, United States. This page reflects FDA report F-0996-2018, dated March 28, 2018.

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 Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.s.a recall?

Avalon Packaging recalled Nxtgen Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.s.a in an FDA Class I enforcement action reported as F-0996-2018. Avalon Packaging is recalling NXTGEN Kratom because of the potential for Salmonella contamination.

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 Avalon Packaging 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-0996-2018. 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

Related alerts

Recent Salmonella recalls

All alerts

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