EYLEA recall: Sterility Concern
EYLEA, (aflibercept) Injection, 2 mg (0.05mL of a 40mg/mL solution), Single-dose Pre-filled Syringe, Rx only, Manufactured by: Regeneron…
Why was EYLEA recalled?
Lack of Assurance of Sterility: Complaints of syringe breakage
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # 8231500321, Exp 10/31 24; 8231500335, 8231500333, 8231500334, 8231500339, 8231500347, Exp 1/30/25
- Product
- EYLEA, (aflibercept) Injection, 2 mg (0.05mL of a 40mg/mL solution), Single-dose Pre-filled Syringe, Rx only, Manufactured by: Regeneron…
- Recalling firm
- Regeneron Pharmaceuticals Inc
- Quantity
- 251,504 syringes
- Distribution
- USA Nationwide
- Recall date
- May 8, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)