Quick Facts at a Glance
- Recall Date
- April 24, 2026
- Hazard Level
- HIGH
- Brands
- LIRAGLUTIDE, Lupin Pharmaceuticals, Inc.
- Geographic Scope
- 1 states
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- LIRAGLUTIDE, Lupin Pharmaceuticals, Inc.
- Model numbers
- Lots: a) WB00097, WB00094, WB00088, Expires: Jul. 2027, WB00103, Expires: Oct. 2027, WC00016, Expires: Dec. 2027 +8 more
- UPC codes
- 70748-346, 70748-346-02, 70748-346-03
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
April 24, 2026
Reported by FDA DRUG
May 27, 2026
RecallRadar source check
June 3, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Presence of particulate matter: a white thread-like structure in the cartridge
What You Should Do
Consumers and healthcare providers should stop using this product immediately. Contact Lupin Pharmaceuticals Inc. or your healthcare provider for guidance. Notification method: Letter
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Full Description
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.. Generic: LIRAGLUTIDE; Brand: LIRAGLUTIDE. Reason: Presence of particulate matter: a white thread-like structure in the cartridge. Classification: Class II. Quantity: 217,621 pen injectors. Distribution: Nationwide within U.S
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Safety Guide
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