Chiesi USA, Inc.: CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension,
Recall reason: Lack of Assurance of Sterility. Recalled by Chiesi USA, Inc.. Distribution: Nationwide within the United States. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot #: 1213748, Exp. Date 09/2026; 1215076, 1215077, Exp. Date 10/26.. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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