Class II · Moderate risk
Eylea
Lack of Assurance of Sterility: Complaints of syringe breakage
Is Aflibercept recalled?
Not under an active recall.
Aflibercept was recalled 3 times in the past — all now closed. Most recent: May 15, 2024.
Most common reason: Sterility / contamination (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Aflibercept. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Aflibercept recalls on record
none so far in 2026; 3 on record, newest first
Class II · Moderate risk
Eylea
Lack of Assurance of Sterility: Complaints of syringe breakage
Class II · Moderate risk
Aflibercept
Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.
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