Regeneron recalls EYLEA (aflibercept) injections due to reported syringe breakage. Affected lots expire by January 2025. Patients should contact the manufacturer for details.
Lack of Assurance of Sterility: Complaints of syringe breakage
Regeneron is recalling EYLEA injections after complaints of syringe breakage. This could lead to injury during eye treatments if the syringe breaks unexpectedly.
Syringe breakage during intravitreal injections could cause injury to the eye. The breakage is reported in complaints but not confirmed as a widespread issue.
Patients receiving EYLEA injections for eye conditions. Those with the specific lot numbers listed in the recall are most at risk.
Check the product label for the lot numbers: 8231500321, 8231500333, 8231500334, 8231500339, 8231500347, 8231500336, 8231500337, 8231500340, 8268700014. The product expires by January 2025.
Look for the lot numbers listed in the recall: 8231500321, 8231500333, 8231500334, 8231500339, 8231500347, 8231500336, 8231500337, 8231500340, 8268700014.
Reach out to Regeneron Pharmaceuticals for further instructions on handling the recalled product.
Regeneron is recalling EYLEA injections after complaints of syringe breakage during intravitreal eye treatments.
The affected lot numbers are 8231500321, 8231500333, 8231500334, 8231500339, 8231500347, 8231500336, 8231500337, 8231500340, and 8268700014.
Check the product label for the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Regeneron to request your refund or repair — edit it as you like.
Subject: Recall D-0531-2024 — Regeneron Regeneron Hello, I own a Regeneron that is covered by recall D-0531-2024 from Regeneron. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.