Nucala (mepolizumab) Injection, 100 mg/mL Prefilled Syringe, Single-Dose, For subcutaneous recall — FDA D-1876-2019
Temperature Abuse; Product stored and shipped outside of labeled storage requirements.
Overview of recall records associated with Cardinal Health dba Specialty Pharmaceutical Services, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Temperature Abuse; Product stored and shipped outside of labeled storage requirements.
This page summarizes recall records in which the official source identifies Cardinal Health dba Specialty Pharmaceutical Services as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.