FDA Drugs recall ·

Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe… recall

Recall number
D-0248-2025
Date
(initiated February 18, 2025)
Company / brand
Turbare Manufacturing
925 Jeanette Dr, Conway, AR, United States
Category
Drugs › Class II
Classification
Class II
Status
Completed
Units affected
1,147 syringes
Hazard tags
Sterility
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

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.

Why was it recalled?

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

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

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

Distribution

Nationwide in the USA

What does Class II mean?

Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.

Source: FDA (drugs), recall D-0248-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.