Reported Oct 2, 2019 · Terminated

Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose, For subcutaneous use only, Rx Only,…

Cardinal Health dba Specialty Pharmaceutical Services

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cardinal Health dba Specialty Pharmaceutical Services · 15 Ingram Blvd · La Vergne, TN · 37086-3630

Is this the product you have?

  • Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose, For subcutaneous use only, Rx Only, Manufactured by GlaxoSmithKline LLC, Philadelphia, PA 19112, Distributed by GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0892-42.
Lot codes and dates
    • Lot #: S25X
    • Exp. 03/31/21
Amount recalled
38 syringes

Where it was sold

  • Nationwide

Why it was recalled

Temperature Abuse; Product stored and shipped outside of labeled storage requirements.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Oct 8, 2020 · Data as of Sep 19, 8:00 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.