Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Trulicity (dulaglutide) Recalled by Eli Lilly & Company Due to Labeling: Label error on declared strength - autoinjector...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Eli Lilly & Company directly.
Affected Products
Trulicity (dulaglutide), 0.75 mg/0.5 mL, 4 Single-Dose Pens per box, Rx only, Eli Lilly and Company, Indianapolis, IN 46285, NDC 0002-1433-80
Quantity: 119,539 4-packs
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Eli Lilly & Company
Eli Lilly & Company has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report