RECALL RECORD — CLASS IIRecall closedF-0412-2019/FDA enforcement

Internal Cleansing Kit Peppermint

What you need to know

Class II
  • What happened

    Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Lead is a toxic heavy metal with no safe blood lead level in children.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDADistribution not listedMore food

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Product identification

Source: FDA FOOD

Brand nameNutranext Business LLC
Recalling firmNutranext Business LLCSunrise, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Batch # SC69 SC69 SC68 SC69 SC68 SC68 SC65 SC66 SC65 SC65 SC629 SC613 SC607 SC587 SC583 SC576 SC566 SC560 SC556 SC543 SC532 SC527 SC519 SC507
Distribution area

US and Foreign Consignees only. No government consignees.

United States

Quantity affected2387 pkgs
Recall initiationFDA report date: November 14, 2018
FDA recall numberF-0412-2019

Beyond the headline

The recall, in context

Nutranext Business LLC initiated this food recall on October 1, 2018. The FDA enforcement report states: Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population. The FDA report lists distribution as: US and Foreign Consignees only. No government consignees.

The FDA enforcement report describes the reason as: Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.

Internal Cleansing Kit Peppermint was made or distributed by Nutranext Business LLC in Sunrise, FL, United States. This page reflects FDA report F-0412-2019, dated November 14, 2018.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, lead is a toxic heavy metal with no safe blood lead level in children.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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

Lead contamination

Possible health effects

Lead can affect the nervous system and is especially harmful to children and pregnant people. Symptoms may include abdominal pain, constipation, fatigue or headaches, but some exposed people have no obvious symptoms.

When symptoms may appear

Health effects depend on the amount and duration of exposure; there is no safe blood lead level in children.

Higher-risk groups

Infants, young children, pregnant people and anyone with repeated exposure are at greatest risk.

What to do now

  1. 1Stop using or eating the affected product and prevent children from handling it.
  2. 2Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal.
  3. 3If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

Do not use home remedies or ignore possible exposure; clinical testing is the appropriate next step.

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 Internal Cleansing Kit Peppermint recall?

Nutranext Business LLC recalled Internal Cleansing Kit Peppermint in an FDA Class II enforcement action reported as F-0412-2019. Routine quality testing identified elevated levels of lead above applicable 2232 levels, which may pose potential health risks to a portion of the population.

What injuries or health effects are linked to lead contamination?

Lead can affect the nervous system and is especially harmful to children and pregnant people. Symptoms may include abdominal pain, constipation, fatigue or headaches, but some exposed people have no obvious symptoms.

How quickly can Lead contamination symptoms appear?

Health effects depend on the amount and duration of exposure; there is no safe blood lead level in children.

Who is most at risk from Lead contamination?

Infants, young children, pregnant people and anyone with repeated exposure are at greatest risk.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the affected product and prevent children from handling it. Keep the packaging and ask the retailer or manufacturer about a refund; follow local guidance for safe disposal. If a child or pregnant person may have been exposed, contact a healthcare professional about blood lead testing.

How do I get a refund from Nutranext Business LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0412-2019 and keep the packaging, lot code and proof of purchase if you have them.

Is the Nutranext Business 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-0412-2019. 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

Brand history

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