Pascalite Powder 8 oz
Recalling firm: Pascalite, Incorporated
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 10, 2013.
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FDA 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.
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Full FDA record and distribution details
Original 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.
Original FDA recall reason
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Recall details
- Recall number
- F-1127-2013
- Event ID
- 64145
- FDA status
- Terminated
- Initiated
- Jan 2, 2013
- Reported
- Mar 27, 2013
- Classified
- Mar 19, 2013
- Terminated
- Apr 10, 2013
- Quantity
- In part of 2,655 units.
- Location
- Worland, WY, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Nationally (U.S.); Canada, UK, Hong Kong, and Australia.
Data updated September 16, 2026. View official FDA data ↗
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