Class II · Moderate risk Completed
Trulicity
Reason TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
Trulicity
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 due to inclement weather.
What was recalled
Trulicity (dulaglutide) injection, 1.5 mg/0.5mL once weekly, 4 Single-Dose Pens, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 00002-1434-80
- Recalling firm
- Cardinal Health Inc.
- NDC code
- 00002-1434-80
- Origin
- OH, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0883-2022
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.
Other Dulaglutide recalls
See all
Class II · Moderate risk Terminated
Trulicity
Reason 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.
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