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FDAFDA · Food and drugs·Recall number D-0005-2025

Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufactured for: Gilead Sciences, Inc., Foster City, CA 94404, NDC 61958-2901-2

Published October 9, 2024 · Recall initiated: September 19, 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

Presence of Particulate Matter: Presence of glass particle.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
VEKLURY
Manufacturer
Gilead Sciences, Inc.
Distributor
Nationwide in the U.S.A.
Lot
Lot: 47035CFA, Exp. 11/2025
Risk classification
Class I
Area (FDA)
drug
Country
United States

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