Turbare Manufacturing Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection recall — FDA D-0248-2025
Lack of Assurance of Sterility: due to a quality control process deviation
Overview of recall records associated with Turbare Manufacturing, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Lack of Assurance of Sterility: due to a quality control process deviation
This page summarizes recall records in which the official source identifies Turbare Manufacturing as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.