FDAFDA · Food and drugs·Recall number D-0479-2024
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
Published May 8, 2024 · Recall initiated: April 23, 2024
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility: Complaints of syringe breakage
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- EYLEA
- Manufacturer
- Regeneron Pharmaceuticals Inc
- Distributor
- USA Nationwide
- Lot
- Lot # 8231500321, Exp 10/31 24; 8231500335, 8231500333, 8231500334, 8231500339, 8231500347, Exp 1/30/25
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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