FDAFDA · Food and drugs·Recall number D-0494-2026
Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL), 5 mL Single-Dose Vial, For intravenous use, Rx Only, American Regent, Inc., Shirley, NY 11967. NDC: 0517-1045-01
Published May 6, 2026 · Recall initiated: April 16, 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
Labeling: Missing Label
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LEVOCARNITINE
- Manufacturer
- American Regent, Inc.
- Distributor
- U.S. Nationwide
- Lot
- Lot 24159N0C0, Exp. June 30, 2026 Lot 25193N0C0, Exp. July 31, 2027
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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