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Class II: temporary or reversible health riskTerminated

Pascalite Powder 8 oz Recall

Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in semitransparent flexible plas…

Pascalite, Incorporated · Worland, WY

Risk level
Class II
Reported by FDA
Mar 27, 2013
Recall ID
F-1127-2013
Check your lot numberHow we source this data

Summary

Pascalite recalled Pascalite Powder 8 oz starting Jan 2, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1127-2013 on Mar 27, 2013. Reason: Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead. Status: Terminated.

Why it was recalled

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

Product description

Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in semitransparent flexible plastic containers with a stick on label. Pascalite Clay Powder, Pascalite Inc, PO Box 104 Worland, WY 82401, 307-347-3872 with directions for use as a Poultice, skin cleanser and softener, deodorant an freshener, dentrifice and oral hygiene, and dietary supplement for adults and children over 6.

Lot numbers, UPCs & expiration 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.

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1127-2013
Classification
Class II
Status
Terminated
Recall initiated
Jan 2, 2013
FDA report date
Mar 27, 2013
Quantity
In part of 2,655 units.
Recall type
Voluntary: Firm initiated
Recalling firm
Pascalite, Incorporated

Original FDA data

Every field from FDA enforcement report F-1127-2013, exactly as published.

Show all FDA fields
City
Worland
State
WY
Status
Terminated
Country
United States
Event ID
64145
Address
329 Lawson Avenue
Code information
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.
Postal code
82401-2045
Report date
Mar 27, 2013
Product type
Food
Recall number
F-1127-2013
Classification
Class II
Recalling firm
Pascalite, Incorporated
Product quantity
In part of 2,655 units.
Termination date
Apr 10, 2013
Reason for recall
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in semitransparent flexible plastic containers with a stick on label. Pascalite Clay Powder, Pascalite Inc, PO Box 104 Worland, WY 82401, 307-347-3872 with directions for use as a Poultice, skin cleanser and softener, deodorant an freshener, dentrifice and oral hygiene, and dietary supplement for adults and children over 6.
Distribution pattern
Nationally (U.S.); Canada, UK, Hong Kong, and Australia.
Recall initiation date
Jan 2, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Mar 19, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1127-2013, published Mar 27, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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