HIGH
FDA DRUG
EPINEPHRINE Injection, USP, 1 mg/10mL (0.1 mg/mL), Rx only, INTERNATIONAL MEDICATION SYSTEMS, LIMITED, So. EL Monte, CA 91733, An Amphastar Pharmaceutical Company, NDC 76329-3318-1
Lack of Assurance of Sterility
EPINEPHRINE
Lack of
EPINEPHRINE Recalls
2 recalls found for EPINEPHRINE. Check if any of your products are affected.
Health & Personal Care
HIGH
FDA DRUG
Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)
Hospira recalls 49,620 vials of Epinephrine Injection, distributed nationwide in the United States. The recall, active since August 4, 2025, targets vials with NDC 0409-4933-05 and case NDC 0409-4933-10. The hazard is lack of assurance of sterility. Health professionals should stop using the product and contact Pfizer or a healthcare provider for guidance.
Epinephrine
Lack of
Brand Statistics
Total Recalls
2
Pages
1