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.

Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.

Recall #: F-1126-2013
Affected scope: In part of 2,655 Units
Initiated: January 2, 2013

Compiled from official public sources by the publisher. · Updated September 2026

Pascalite, Incorporated recalled Pascalite Capsules 100 count white plastic bottle with a screw on top, Pascalite Inc, PO … - a moderate-severity action.

Pascalite Capsules 100 count white plastic bottle with a screw on top, Pascalite Inc, PO … 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-1126-2013 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….

Moderate
severity level: Class II
classification: March 27, 2013
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1126-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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 - 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 agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.

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.

Reason for recall

Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-1126-2013
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.

Check the recall number (F-1126-2013) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

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.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.

Which agency issued this recall? ▼

This recall was issued by the FDA Food on March 27, 2013. Severity: Moderate. Recall number: F-1126-2013.

Where was the recalled product distributed? ▼

Distribution: Nationally (U.S.); Canada, UK, Hong Kong, and Australia..

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nationwide recalls with similar severity or category timing

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Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

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Same product category, closest by report date among other firms and states (deduped against the severity set).

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This recall: FDA Food, reported March 27, 2013. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026