SUN PHARMACEUTICAL INDUSTRIES INC — FDA Class II (D-0628-2026)

SUN PHARMACEUTICAL INDUSTRIES INC is recalling 3,456 bottles of a human medication due to a labeling mix-up. The recall is due to incorrect labeling of the 10mg dosage. This is a Class II recall, indicating a temporary health issue.

• •SUN PHARMACEUTICAL INDUSTRIES INC is recalling 3,456 bottles of a medication.
• •The recall is due to a labeling mix-up for the 10mg dosage.
• •This is classified as a Class II recall.
• •Consumers should check their medicine cabinets for affected products.
• •Recall actions like this are taken to prevent potential health risks.

Consumers who have these bottles should stop using them and contact the firm for further instructions. The labeling issue could lead to incorrect medication usage.