Drug recall D-0773-2021
Product
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
Reason for recall
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.
Lots and codes
Lot number: D396436C
Recall details
- Recalling firm
- Eli Lilly & Company, Indianapolis, IN
- Quantity
- 119,539 4-packs
- Distribution
- USA Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 19, 2021
- Terminated
- August 7, 2023
Related products
- Trulicity – drug information
- NDC 0002-3182 Trulicity · Dulaglutide 4.5 mg/.5mL · Eli Lilly and Company
- NDC 0002-2236 Trulicity · Dulaglutide 3 mg/.5mL · Eli Lilly and Company
- NDC 0002-1433 Trulicity · Dulaglutide .75 mg/.5mL · Eli Lilly and Company
- NDC 0002-1434 Trulicity · Dulaglutide 1.5 mg/.5mL · Eli Lilly and Company