Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing Due to Lack of Assurance of Sterility: due to a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Turbare Manufacturing directly.
Affected Products
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.
Quantity: 1,147 syringes
Why Was This Recalled?
Lack of Assurance of Sterility: due to a quality control process deviation. During an internal quality assurance review, an Acceptable Quality Limit (AQL) inspection was not conducted on a statistically sound number of samples. This may result in the inability to assure that the impacted products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess and may lead to products of unacceptable quality.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Turbare Manufacturing
Turbare Manufacturing has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report