Drug recall D-0577-2021
Product
EPINEPHRINE INJECTION USP, 0.3MG (AUTO-INJECTORS) FOR ALLERGIC EMERGENCIES (ANAPHYLAXIS) 2 Auto-Injectors and 1 Trainer, Manufactured for: Teva Pharmaceuticals USA, Inc., North Wales, PA 19454 NDC 0093-5986-27
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
033J20AA
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 414 boxes
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Epinephrine – drug information
- NDC 0093-5985 Epinephrine · Epinephrine .15 mg/.3mL · Teva Pharmaceuticals USA, Inc.
- NDC 0093-5986 Epinephrine · Epinephrine .3 mg/.3mL · Teva Pharmaceuticals USA, Inc.