Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
What was recalled
Trulicity (dulaglutide) injection, 0.75 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 0002-1433-80
Recalling firm
Cardinal Health Inc.
NDC code
0002-1433-80
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0884-2022
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.