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Class I: serious health riskTerminated

Gilead Sciences Veklury Recall

Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial, Rx only, Manufacture…

Gilead Sciences, Inc. · Foster City, CA

Risk level
Class I
Reported by FDA
Oct 9, 2024
Recall ID
D-0005-2025
Check your lot numberHow we source this data

Summary

Gilead Sciences recalled Veklury starting Sep 19, 2024. The FDA classified it as Class I (serious health risk) and published enforcement report D-0005-2025 on Oct 9, 2024. Reason: Presence of Particulate Matter: Presence of glass particle. Status: Terminated.

Why it was recalled

Presence of Particulate Matter: Presence of glass particle.

Product description

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

Lot numbers, UPCs & expiration codes

Lot: 47035CFA, Exp. 11/2025

Where it was sold

Nationwide in the U.S.A.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0005-2025
Classification
Class I
Status
Terminated
Recall initiated
Sep 19, 2024
FDA report date
Oct 9, 2024
Quantity
105,000 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Gilead Sciences, Inc.

Original FDA data

Every field from FDA enforcement report D-0005-2025, exactly as published.

Show all FDA fields
City
Foster City
State
CA
Status
Terminated
Country
United States
Event ID
95399
Address
333 Lakeside Dr
Code information
Lot: 47035CFA, Exp. 11/2025
Postal code
94404-1147
Report date
Oct 9, 2024
Product type
Drugs
Recall number
D-0005-2025
Classification
Class I
Recalling firm
Gilead Sciences, Inc.
Product quantity
105,000 vials
Termination date
Jul 29, 2025
Reason for recall
Presence of Particulate Matter: Presence of glass particle.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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
Distribution pattern
Nationwide in the U.S.A.
Recall initiation date
Sep 19, 2024
Initial firm notification
Letter
Center classification date
Oct 3, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0005-2025, published Oct 9, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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