Class II
Drug Recall: 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 Driv
Turbare Manufacturing · February 18, 2025
Reason for Recall
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.
Distribution
Nationwide in the USA
States Affected
NATIONWIDE
Quantity Affected
1,147 syringes
Source: FDA (openFDA Drug Enforcement)
Recall number: D-0248-2025
Status: completed
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.