Turbare Manufacturing
Turbare Manufacturing appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 1 compliance action on record. Its most recent recall (D-0248-2025, Class II) was initiated on February 18, 2025.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 1
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-0248-2025 | Class II | Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not f | February 18, 2025 |