FDA Drugs recall ·
Veklury (remdesivir) for injection, 100 mg/vial, Single-Dose Vial… recall
This is an FDA Class I recall — the most serious type.
Read the official FDA notice ↗
Product
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
Why was it recalled?
Presence of Particulate Matter: Presence of glass particle.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot: 47035CFA, Exp. 11/2025
Distribution
Nationwide in the U.S.A.
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0005-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.