Drug recall D-0402-2026
Product
CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.
Reason for recall
Lack of Assurance of Sterility
Lots and codes
Lot #: 1213748, Exp. Date 09/2026; 1215076, 1215077, Exp. Date 10/26.
Recall details
- Recalling firm
- Chiesi USA, Inc., Cary, NC
- Quantity
- 7,235 vials
- Distribution
- Nationwide within the United States
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 17, 2026
Related products
- Curosurf – drug information
- NDC 10122-510 Curosurf · Poractant Alfa 80 mg/mL · Chiesi USA, Inc.