Chiesi USA, Inc. recalls CLEVIPREX (clevidipine injectable emulsion) 50 mg/100 mL (0.
See all recalls from Chiesi USA, Inc. →Recalled Product
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.
Hazard / Issue
Lack of Assurance of Sterility
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 1239521, 1237454, Exp. Date 10/2027
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for CLEVIPREX (clevidipine injectable emulsion) →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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