US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 23, 2024 (2 years ago)

EYLEA, (aflibercept) Injection, 2 mg (0.05mL of a 40mg/mL solution), Single-dose…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility: Complaints of syringe breakage

What was recalled

EYLEA, (aflibercept) Injection, 2 mg (0.05mL of a 40mg/mL solution), Single-dose Pre-filled Syringe, Rx only, Manufactured by: Regeneron Pharmaceuticals, Inc., 777 Old Saw Mill River Road, Tarrytown, NY 10591, NDC 61755-005-01

Recalling firm
Regeneron Pharmaceuticals Inc
NDC code
61755-005-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0479-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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