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 U
Recalled March 5, 2025 · FDA recall D-0248-2025 · Turbare Manufacturing
Hazard
Lack of Assurance of Sterility: due to a quality control process deviation · FDA Class II
Units
1,147 syringes
Sold at
Nationwide in the USA
Description
Lack of Assurance of Sterility: due to a quality control process deviation
Product
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.
Manufacturer(s)
Turbare Manufacturing
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →