Pascalite Capsules
Reason Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Pascalite Powder recall
Recalled by Pascalite, Incorporated · Worland, WY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Some of these cause harm only with repeated exposure (lead in spices, for example), others act within hours (histamine poisoning from spoiled fish). All chemical contamination recalls.
What was recalled
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.
Quantity: In part of 2,655 units.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
FDA's distribution note: Nationally (U.S.); Canada, UK, Hong Kong, and Australia.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Pascalite, Incorporated
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 2, 2013
- In FDA report of
- Mar 27, 2013
- Terminated
- Apr 10, 2013
- FDA recall number
- F-1127-2013 · event 64145
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.