Gilead Veklury injection recall: Glass particles risk serious injury

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Contact the company & request your remedy

Recalling firmGilead Sciences, Inc.333 Lakeside Dr, N/A · Foster City, CA 94404-1147

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Gilead is recalling Veklury injections because they may contain glass particles that could cause serious injury. This affects patients receiving the medication for certain infections. If you have this product, stop using it immediately.

Why it’s dangerous

Glass particles in the injection vial could cause serious injury when injected, such as tissue damage or infection. This is a critical safety issue for patients receiving the medication.

Who’s affected

Patients prescribed Veklury injections for specific infections. Those with the lot number 47035CFA (expiring 11/2025) are most at risk.

How to tell if you have this one

Check the vial label for the lot number 47035CFA and expiration date 11/2025. The product is a 100 mg/vial injection for medical use only.

Brand
Gilead
Category
Drug

Based on the official FDA remedy

What to do — step by step

Stop Using Immediately
Discard the vial if you have the lot number 47035CFA or expiration date 11/2025.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

No, the product may contain glass particles that could cause serious injury. Do not use.

What should I do if I have this product?

Discard the vial immediately if you have the lot number 47035CFA or expiration date 11/2025.

How can I check if I have the recalled product?

Check the vial label for the lot number 47035CFA and expiration date 11/2025.

Take action

Contact Gilead

We’ve drafted a message you can send Gilead to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-0005-2025 — Gilead Gilead

Hello,

I own a Gilead that is covered by recall D-0005-2025 from Gilead.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #D-0005-2025 (September 19, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0005-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

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