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Chiesi USA, Inc. Recalls

2 recalls found for Chiesi USA, Inc.. Check current safety alerts and related brands before using affected products.

Active recalls: 2
Pages: 1

HIGH

FDA DRUG

CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.5 mg/mL), 10 Single Use Vials, Rx Only, Manufactured for: Chiesi USA, Inc., Cary, NC 27518, by Fresenius Kabi, Graz, Austria, NDC...

Lack of Assurance of Sterility

Jul 6, 2026

CLEVIPREX

Lack of

Health & Personal Care

HIGH

FDA DRUG

Curosurf 240 mg Poractant Alfa Recalled for Sterility Concerns (2026)

Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.

Mar 17, 2026

CUROSURF

Lack of

Brand Statistics

Total Recalls

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Related Brands

CLEVIPREX CUROSURF