Pascalite Capsules (Pascalite) – lead contamination (2013)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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.
Brand
Pascalite, Incorporated
Lot Codes / Batch Numbers
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.
Products Sold
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.
Pascalite, Incorporated is recalling Pascalite Capsules 100 count white plastic bottle with a screw on top, Pascalite Inc, PO Box 104 Wor due to Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Pascalite is recalling internally used pascalite powder products because they may contain violative levels of lead.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026