Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported March 27, 2013
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.
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 FDA Food action (record #F-1126-2013) 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 - 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.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products 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.
Affected scope
In part of 2,655 Units
Related Recalls
6
0 from same agency
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
| 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? ▼
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.. Recalled by Pascalite, Incorporated. Units affected: In part of 2,655 Units.
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..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1126-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
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.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
CPSC Moderate
AMASKY Nursing Pillows Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards fo…
Xishentang Dongguan Trading Co, Ltd., dba Pretty-Life, of China · 2026-07-02
CPSC Moderate
Diamond Wipes International Recalls CVS Health Medicated Hemorrhoidal Wipes Due to Risk of Serious Injury or Death from…
Diamond Wipes International, Inc. of Chino, California · 2026-07-02
CPSC Moderate
Junpower CR2032 Lithium Coin Batteries Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; V…
· 2026-07-02
CPSC Moderate
Target Recalls Gigglescape™ Under the Sea Popping Toy Due to Choking Hazard
· 2026-07-02
CPSC Moderate
Vevor Recalls Baby Loungers Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory …
Sanven Technology Ltd., dba Vevor, of Rancho Cucamonga, California · 2026-07-02
Compare this recall with AMASKY Nursing Pillows Recalled Due to Risk of Serious Inju… →
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.