FDAFDA · Food and drugs·Recall number D-0248-2025
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.
Published March 5, 2025 · Recall initiated: February 18, 2025
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: due to a quality control process deviation
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Turbare Manufacturing
- Distributor
- Nationwide in the USA
- Lot
- Lot #s: 12122024@2 (BUD: 3/12/2025); 12192024@2 (BUD: 4/18/2025).
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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