Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug produ…
Turbare Manufacturing · Lack of Assurance of Sterility: due to a quality control process deviation
- Status
- Terminated
- City
- Conway
- State
- AR
- Country
- United States
- Classification
- Class II
- Product type
- Drugs
- Event ID
- 96306
- Recalling firm
- Turbare Manufacturing
- Address 1
- 925 Jeanette Dr
- Address 2
- N/A
- Postal code
- 72032-6651
- Voluntary mandated
- Voluntary: Firm initiated
- Initial firm notification
- Distribution pattern
- Nationwide in the USA
- Recall number
- D-0248-2025
- Product quantity
- 1,147 syringes
- Reason for recall
- Lack of Assurance of Sterility: due to a quality control process deviation
- Recall initiation date
- 20250218
- Center classification date
- 20250221
- Termination date
- 20260226
- Report date
- 20250305
- Code info
- Lot #s: 12122024@2 (BUD: 3/12/2025); 12192024@2 (BUD: 4/18/2025).
- Product description
Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single Use, This drug product was repackaged by Turbare Manufacturing, 925 Jeanette Drive, Conway, AR 72032, NDC: 83556-0101-01.