Recall
FDAHealthFebruary 18, 2025

Turbare Manufacturing — 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 Manufact

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
February 18, 2025

Nationwide in the USA

What's affected?

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.
Lot code
12122024@2

Additional details

Lot #s: 12122024@2 (BUD: 3/12/2025); 12192024@2 (BUD: 4/18/2025).

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 1,147 syringes.

View original FDA notice →

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