FDAFDA · Food and drugs·Recall number D-0503-2024
niCARdipine Hydrochloride Injection, USP, 25 mg/10 mL (2.5 mg/mL), 10 x 10 mL Single Dose Vials, Rx Only, For Intravenous Use Only, Mfd for: Civica, Inc., Lehi, UT 84043; Mfd by: American Regent, Inc., New Albany, OH 43054. NDC 72572-470-10
Published May 29, 2024 · Recall initiated: May 14, 2024
Status when published: Terminated — 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
- NICARDIPINE HYDROCHLORIDE
- Manufacturer
- American Regent, Inc.
- Distributor
- UT only
- Lot
- Lot #: 23087N0C0, Exp. Date 11/2024
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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