Overview of recall records associated with Eli Lilly & Company, including dates, categories and classifications where available.
Classification mix: Class II: 2, Class I: 1.
SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected powder substance. There was also a lack of full drug effect upon administration.
Labeling: Label error on declared strength - autoinjector devices labeled as 0.75 mg / 0.5 mL actually contain 1.5 mg / 0.5 mL of product.
cGMP deviations: Atypical appearance, decrease in size and change in color of the lyophilized cake of drug product.
This page summarizes recall records in which the official source identifies Eli Lilly & Company 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.
