FDA Drug Recalls

Recalls / Brands / Curosurf

Curosurf

1 FDA drug recall involving brand “Curosurf.

DateClassProductFirm
2026-03-17Class IICUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, CaChiesi USA, Inc.