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RECALL RECORD — CLASS IIRecall closedF-1127-2013/FDA enforcement
Pascalite, Incorporated·Cosmetics·Jan 2, 2013

Pascalite Powder 8 OZ, 16 OZ, 5 lb, and 25 lb Packaged in Semitransparent Flexible Plastic…

What you need to know

Class II

  • What happened

    Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.

  • 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

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall closed · classified by the FDADistribution not listedMore cosmetics

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Product identification

Source: FDA FOOD

Brand namePascalite, Incorporated
Recalling firmPascalite, IncorporatedWorland, WY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot numbers imprinted or hand written include: 2010M
  • and D10 through 12 with a noted OT, U, V, or W. The code information is found on the bottom of the product.
Distribution area

Nationally (U.S.); Canada, UK, Hong Kong, and Australia.

United States, Canada, United Kingdom, Australia

Quantity affectedIn part of 2, 655 units.
Recall initiationFDA report date: March 27, 2013
FDA recall numberF-1127-2013

Beyond the headline

The recall, in context

Pascalite, Incorporated initiated this cosmetics recall on January 2, 2013. The FDA enforcement report states: Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead. The FDA report lists distribution as: Nationally (U.S.); Canada, UK, Hong Kong, and Australia.

The FDA enforcement report describes the reason as: Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.

Pascalite Powder 8 OZ, 16 OZ, 5 lb, and 25 lb Packaged in Semitransparent Flexible Plastic… was made or distributed by Pascalite, Incorporated in Worland, WY, United States. This page reflects FDA report F-1127-2013, dated March 27, 2013.

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

    Set the product aside and do not apply it.

  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 Pascalite Powder 8 OZ, 16 OZ, 5 lb, and 25 lb Packaged in Semitransparent Flexible Plastic… recall?

Pascalite, Incorporated recalled Pascalite Powder 8 OZ, 16 OZ, 5 lb, and 25 lb Packaged in Semitransparent Flexible Plastic… in an FDA Class II enforcement action reported as F-1127-2013. Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.

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?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. 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 Pascalite, Incorporated?

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-1127-2013 and keep the packaging, lot code and proof of purchase if you have them.

Is the Pascalite, Incorporated 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-1127-2013. 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

More recalls by Pascalite, Incorporated

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