Severity
Moderate
FDA Food recall · Reported March 27, 2013
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Pascalite, Incorporated recalled Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in semitransparent flexible plasti… - a moderate-severity action.
Pascalite Powder 8 oz, 16 oz, 5 lb, and 25 lb packaged in semitransparent flexible plasti… was recalled by Pascalite, Incorporated in March 27, 2013. Reason: Pascalite is recalling internally used pascalite powder products because they may contain violative levels of…. Check the official notice for the remedy. Verify recall #F-1127-2013 with the FDA Food before acting.
The recall
Pascalite, Incorporated issued this moderate-severity FDA Food recall-Pascalite is recalling internally used pascalite powder products because they may contain violative levels of….
Sourced from official FDA Food enforcement records. Verify recall #F-1127-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1127-2013) was formally reported on March 27, 2013, with the manufacturer initiating the action on January 2, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Pascalite, Incorporated is listed as the recalling firm, operating out of Worland, WY. Federal records list the affected scope as In part of 2,655 units..
The documented reason for this recall is: Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead. Distribution data in the federal record shows the product reached: Nationally (U.S.); Canada, UK, Hong Kong, and Australia.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 1,360 cosmetics & personal care recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
In part of 2,655 units.
Related Recalls
6
2 from same agency
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.
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1127-2013 |
| Date reported | March 27, 2013 |
| Date initiated | January 2, 2013 |
| Recalling firm | Pascalite, Incorporated |
| Firm location | Worland, WY |
| Affected scope | In part of 2,655 units. |
| Distribution | Nationally (U.S.); Canada, UK, Hong Kong, and Australia. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported March 27, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.