FDAFDA · Food and drugs·Recall number D-0689-2026
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 10122-611-10.
Published July 22, 2026 · Recall initiated: July 6, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Lack of Assurance of Sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- CLEVIPREX
- Manufacturer
- Chiesi USA, Inc.
- Distributor
- Nationwide within the United States
- Lot
- Lot #: 1239521, 1237454, Exp. Date 10/2027
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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