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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Drug
Medications & Supplements/Prescription Drugs

Veklury (remdesivir) Recalled Due to Glass Particulates

Agency Publication Date: December 28, 2021
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Summary

Gilead Sciences, Inc. has voluntarily recalled 53,473 vials of Veklury (remdesivir) for injection, 100 mg/vial. The recall was initiated following a customer complaint and an investigation that confirmed the presence of glass particulates within the medication. This drug is an antiviral medication administered by healthcare providers in hospital settings via intravenous injection. To date, no incidents or injuries have been reported in connection with this recall.

Risk

If glass particulates are present in an injectable medication, they can be introduced into the bloodstream and travel to vital organs. This can lead to serious or life-threatening inflammation or injury in the heart, lungs, or brain. No reports of injuries have been received.

What You Should Do

  1. This recall affects Veklury (remdesivir) for injection, 100 mg/vial, packaged in single-dose vials under NDC 61958-2901-2 with lot numbers 2141001-1A or 2141002-1A and an expiration date of 01/2024.
  2. Stop using the recalled product. Contact Gilead Sciences or your distributor to arrange for the return of any remaining vials.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return.

Affected Products

Product: Veklury (remdesivir) for injection (100 mg/vial)by Veklury
Variants: 100 mg/vial, Single-Dose Vial, Rx only
Lot Numbers:
2141001-1A (Exp. 01/2024)
2141002-1A (Exp. 01/2024)
NDC:
61958-2901-2

Quantity: 53,473 vials

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89153
Status: Resolved
Manufacturer: Gilead Sciences, Inc.
Sold By: hospitals; pharmacies
Manufactured In: United States
Units Affected: 53,473 vials
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.