Avastin 1 recalled over sterility concerns

Recall date

February 18, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Turbare Manufacturing recalls Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection Only, Office Use Only - Not for Resale - Single…

Recall number

D-0248-2025

FDA classification

Class II

Brand / firm

Turbare Manufacturing

Sold / distributed

Nationwide in the USA

Why it was recalled

Lack of Assurance of Sterility: due to a quality control process deviation

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.