Pascalite Capsules 100 count white plastic bottle with a screw on top, Pascalite Inc, PO Box…
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 Capsules 100 count white plastic bottle with a screw on top, Pascalite Inc, PO Box 104 Worland, WY 82401 307-347-3872, Dietary Supplement for adults and children over 12 years two capsules daily, each vegi cap (size 00) contains approx. 1/4 tsp pascalite powder.
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-1126-2013
- 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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