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Class II · ModerateActive recall

Liraglutide

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLots: a) WB00097, WB00094, WB00088, Expires: Jul. 2027; WB00103, Expires: Oct. 2027; WC00016, Expires: Dec. 2027; b) WB00098, WB00092, WB00093, Expires: Jul. 2027; WB00104, WB00106, WB00105, Expires: Oct. 2027.
Where it was soldNationwide within U.S
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byLupin Limited, Nagpur 441108, INDIA, a) 2 Pens- foreign manufacturer
Brand nameLIRAGLUTIDE
Generic nameLIRAGLUTIDE
Active ingredient(s)LIRAGLUTIDE
Distributed by / forLupin Pharmaceuticals, Inc., Naples, FL 34108
NDC70748-346-02
Show the full FDA record
Full product labelLiraglutide 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.
Recalling firmLupin Pharmaceuticals Inc.
DistributionNationwide within U.S
Quantity217,621 pen injectors
Recall initiated2026-04-24
Report date2026-05-27
Recall completed
Recall numberD-0541-2026
ClassificationClass II
FDA statusOngoing
Origin on fileNaples FL United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.