Drug Recall: Eptifibatide Injection Due to Failed Degradation Specifications
Eugia US LLC is recalling 15,500 vials of Eptifibatide injection nationwide due to failed impurities and degradation specifications. The defect involves a related substance identified as Eptifibatide dimer.
- Product
- EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
- Category
- Drug
- Distribution
- Distributed nationwide