Official recall notice
FDA DrugClass IINotable
FDA Recall: CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi US
- Recall date
- 2026-04-01
- Brand
- Chiesi USA, Inc.
- Category
- Drug
- FDA class
- Class II
Why it was recalled
Hazard
Lack of Assurance of Sterility
Recommended action
What to do
7,235 vials
Product description
Lack of Assurance of Sterility