Why it was recalled
Lack of Assurance of Sterility: due to a quality control process deviation
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.
Lot numbers, UPCs & expiration codes
Lot #s: 12122024@2 (BUD: 3/12/2025); 12192024@2 (BUD: 4/18/2025).
Where it was sold
Nationwide in the USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0248-2025
- Classification
- Class II
- Status
- Completed
- Recall initiated
- Feb 18, 2025
- FDA report date
- Mar 5, 2025
- Quantity
- 1,147 syringes
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Turbare Manufacturing
Original FDA data
Every field from FDA enforcement report D-0248-2025, exactly as published.
Show all FDA fields
- City
- Conway
- State
- AR
- Status
- Completed
- Country
- United States
- Event ID
- 96306
- Address
- 925 Jeanette Dr
- Code information
- Lot #s: 12122024@2 (BUD: 3/12/2025); 12192024@2 (BUD: 4/18/2025).
- Postal code
- 72032-6651
- Report date
- Mar 5, 2025
- Product type
- Drugs
- Recall number
- D-0248-2025
- Classification
- Class II
- Recalling firm
- Turbare Manufacturing
- Product quantity
- 1,147 syringes
- Termination date
- Feb 26, 2026
- Reason for recall
- Lack of Assurance of Sterility: due to a quality control process deviation
- Voluntary / mandated
- Voluntary: Firm initiated
- 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.
- Distribution pattern
- Nationwide in the USA
- Recall initiation date
- Feb 18, 2025
- Initial firm notification
- Center classification date
- Feb 21, 2025