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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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