Skip to main content
Recall Canary
Liraglutide Injection
← Back to all recalls
DRUG RECALLMODERATE

Liraglutide Injection

Lupin is recalling Liraglutide Injection (NDC 70748-346-02 and 70748-346-03) due to white thread-like particulate matter in the cartridge.

What to do

Inspect your medication for any visible particles. If you identify a white thread-like structure, do not use the product and contact your healthcare provider or pharmacist for a replacement.

Posted
Updated
Recall No.
D-0541-2026
Agency
Firm
Lupin Pharmaceuticals Inc.
Recall ID
98809
Status
ONGOING

Why it was recalled

Presence of particulate matter: a white thread-like structure in the cartridge

How to identify it

Liraglutide Injection, 18 mg/3 mL (6 mg/mL), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Naples, FL 34108, Manufactured by: Lupin Limited, Nagpur 441108, INDIA, a) 2 Pens- NDC 70748-346-02; b) 3 Pens - NDC 70748-346-03.

Where it was sold

Distributed in US.

← Back to all recalls

Editorial summary by Recall Canary · last updated 2026-05-20 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification