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Drug Recalls

Last updated

Every drug recall in FDA enforcement reports from the last three years, plus older recalls that are still open. Filter by severity, status or medicine, and check the lot numbers on your package.

0 Class I (most serious) drug recalls reported in the last 30 days.

1 recall

  • Class II Terminated

    Sofosbuvir and Velpatasvir, 400 mg/100 mg tablets, 28 tablets: 2×14 blister cards, Rx Only, Manufactured for: Asegua Therapeutics LLC an affiliate of Gilead Sciences, Inc., Foster City, CA 94404, Made in Ireland, NDC# 72…

    Reason: Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton.

    ASEGUA THERAPEUTICS LLC · Velpatasvir and Sofosbuvir

    Lots, distribution and details
    Product
    Sofosbuvir and Velpatasvir, 400 mg/100 mg tablets, 28 tablets: 2×14 blister cards, Rx Only, Manufactured for: Asegua Therapeutics LLC an affiliate of Gilead Sciences, Inc., Foster City, CA 94404, Made in Ireland, NDC# 72626-2701-1
    Lots / codes
    Lot# 24ASV002UA, Exp Date: 6/30/2028
    Distribution
    US Nationwide
    Quantity
    18,541 cartons.
    Recall started
    March 7, 2025 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0313-2025

Have this medicine at home? Compare the lot number and expiry date on your package with the recall. Do not stop taking a prescribed medicine on your own — stopping suddenly can be riskier than the recalled lot. Your pharmacist can check it and usually swap it for an unaffected one.

What the recall classes mean

  • Class I Most serious: use could cause serious health problems or death.
  • Class II Could cause temporary or medically reversible health problems; serious harm is unlikely.
  • Class III Not likely to cause health problems — for example a labelling or packaging fault.

Source: FDA Enforcement Report, via openFDA. Updated here twice a day; last update October 31, 2026 14:40. openFDA data are not validated for clinical use — confirm with the FDA source or your pharmacist.

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