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Chiesi USA, Inc. recall (Cls II)

April 1, 2026updated 5mo ago
community read0 votes

CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03. — Reason: Lack of Assurance of Sterility — Status: Ongoing

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same company · ±60 days · 1

  • approvalJUXTAPID (LOMITAPIDE MESYLATE) — FDA approvalFeb 25, 2026

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