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
Reported: September 1, 2021 Initiated: August 19, 2021 #D-0773-2021
Product Description
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.
Details
- Recalling Firm
- Eli Lilly & Company
- Units Affected
- 119,539 4-packs
- Distribution
- USA Nationwide
- Location
- Indianapolis, IN
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Eli Lilly & Company. Units affected: 119,539 4-packs.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 1, 2021. Severity: Moderate. Recall number: D-0773-2021.
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