Procrit (epoetin alfa)
Presence of particulate matter: glass flakes identified as lamellae observed during a routine quality inspection.
Most common reason: Particulate / foreign matter (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Epoetin. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Presence of particulate matter: glass flakes identified as lamellae observed during a routine quality inspection.
Presence of particulate matter: Visible glass flakes identified as lamellae in some drug product vials.
Presence of Particulate Matter: glass delamination
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