Eugia US LLC — FDA Class III (D-0552-2026)

Eugia US LLC is recalling 168,300 vials of a human prescription drug due to labeling issues. This recall is classified as a voluntary action. The affected product is intended for epidural, infiltration, and intra-articular use.

• •Eugia US LLC is recalling 168,300 vials of a human prescription drug.
• •The recall is due to mislabeling issues.
• •The drug is administered via epidural, infiltration, or intra-articular routes.
• •Patients should check their medicine cabinets for the recalled vials.

Patients who received this drug should verify if they have the recalled vials. The recall affects 168,300 vials due to labeling issues.