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Meridian Medical Technologies a Pfizer Company
FDA Regulatory Profile
Summary
- Total Recalls
- 3 (2 Class I)
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| D-0691-2017 | Class I | EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P | March 12, 2017 |
| D-0690-2017 | Class I | EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Mo | March 12, 2017 |
| D-1369-2012 | Class II | Diazepam Injection, USP, 10 mg Automatic, Autoinjector for Buddy Use, 5 mg/mL, 2 mL autoinjector, 15 | June 6, 2012 |