CLASS II Food recall · Reported 27 Mar 2013 · FDA Enforcement Report
Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged recalled
Pascalite, Incorporated is recalling Pascalite Powder, distributed nationwide in the US. The recall was initiated on 2 Jan 2013 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1127-2013
- FDA event ID
- 64145
- Recalling firm
- Pascalite, Incorporated, Worland, WY
- Brand
- Pascalite
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 2 Jan 2013
- FDA classified
- 19 Mar 2013
- Reported
- 27 Mar 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Foreign Material
- Product category
- Dietary Supplements
Timeline
| 2 Jan 2013 | Recall initiated by company | |
| 19 Mar 2013 | Classified by FDA | +76 days |
| 27 Mar 2013 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
Product as listed by the FDA
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.
Where it was distributed
Nationally (U.S.); Canada, UK, Hong Kong, and Australia.
Questions about this recall
Is Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in recalled?
Yes. Pascalite, Incorporated recalled Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in on 2 Jan 2013. The recall is Class II and its status is Terminated. Recall number F-1127-2013.
Why was it recalled?
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Which lots are affected?
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 was it sold?
Nationally (U.S.); Canada, UK, Hong Kong, and Australia.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Pascalite, Incorporated
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | Capsules white with a screw on top, Pascalite Inc recalledPascalite | Pascalite, Incorporated | Foreign Material | Nationwide |
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| Food | ANNOUNCED | Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali | Global Mix | Foreign Material | Nationwide |
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| Food | CLASS II | Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island | Mellish Island | Other | Nationwide |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |