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RECALL RECORD — CLASS IIIRecall closedF-1121-2024/FDA enforcement
Nicomex INC.·Food·Feb 15, 2024

Nicomex Tequesquite, NET WT

What you need to know

Class III

  • What happened

    Elevated lead levels

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 FDAIN, NJ, NYMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNicomex INC.
Recalling firmNicomex INC.Passaic, NJ, United States
UPC / barcodes
8 84678 10180 7
Lot / date codesNo lot code listed. Follow the recall notice and check the packaging.
Distribution area
INNJNY

Distributed to distributors in NJ, then further distributed to retail stores in NJ and NY.

United States

Quantity affectedApproximately 192 units
Recall initiationFDA report date: April 17, 2024
FDA recall numberF-1121-2024

Beyond the headline

The recall, in context

Nicomex INC. initiated this food recall on February 15, 2024. The FDA enforcement report states: Elevated lead levels. The FDA report lists distribution as: Distributed to distributors in NJ, then further distributed to retail stores in NJ and NY.

The FDA enforcement report describes the reason as: Elevated lead levels

Nicomex Tequesquite, NET WT was made or distributed by Nicomex INC. in Passaic, NJ, United States. This page reflects FDA report F-1121-2024, dated April 17, 2024.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, lead is a toxic heavy metal with no safe blood lead level in children.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 UPC and lot code 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 Nicomex Tequesquite, NET WT recall?

Nicomex INC. recalled Nicomex Tequesquite, NET WT in an FDA Class III enforcement action reported as F-1121-2024. Elevated lead levels

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 Nicomex INC.?

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-1121-2024 and keep the packaging, lot code and proof of purchase if you have them.

Is the Nicomex INC. 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-1121-2024. 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.