Keystone Industries — FDA Class II (D-0605-2026)

Keystone Industries is recalling 450 units of a human over-the-counter drug containing benzocaine due to defective containers. The recall is classified as a safety issue. The affected product is distributed in the United States.

• •Keystone Industries is recalling 450 units of a benzocaine dental product.
• •The recall is due to defective containers that may contain faulty bottles.
• •This recall is classified as a Class II safety issue.
• •Consumers should check their medicine cabinets for the recalled units.

Consumers who have purchased this product should stop using it and check for the 450 recalled units. The defective containers may pose safety risks.