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RECALLING FIRM / COMPANY

Pascalite, Incorporated Recalls

Are there any recent FDA recalls involving Pascalite, Incorporated?

0 recall records initiated in the snapshot’s last 365 days. 0 are FDA-listed ongoing with no termination date.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026

The FDA identifies this company as the recalling firm; this does not establish that it is the manufacturer, retailer or brand owner. “Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today.

2 FDA product recordsLatest initiation: Jan 2, 2013

Same product name.
Different batch.
Check the label.

All FDA recall records involving Pascalite, Incorporated

Initiated in 2013. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

2 recall recordsPage 1 of 1
Class II
FDA status: Terminated

Pascalite Capsules 100 count white plastic bottle with a screw on top, Pascalite Inc, PO Box 104 Worland, WY 82401…

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

Lead / heavy metalsView details →
Class II
FDA status: Terminated

Pascalite Powder 8 oz

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

Lead / heavy metalsView details →

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Same product name. Different batch. Details matter.

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