Recall Ledger

Libtayo recall (Regeneron Pharmaceuticals Inc)

DrugClass IIOngoing

Summary: Regeneron Pharmaceuticals Inc is recalling Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution, Single-Dose Vial, Rx only, Manufactured by: Regeneron Pharmaceuticals, Inc., Tarrytown, NY 10591; Marketed by: Regeneron Pharmaceuticals, Inc. (Tarrytown, NY 10591), NDC 61755-008-01. Reason: Lack of Assurance of Sterility.

What is being recalled

Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution, Single-Dose Vial, Rx only, Manufactured by: Regeneron Pharmaceuticals, Inc., Tarrytown, NY 10591; Marketed by: Regeneron Pharmaceuticals, Inc. (Tarrytown, NY 10591), NDC 61755-008-01

Why

Lack of Assurance of Sterility

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

USA Nationwide

How to tell if yours is affected

Lot: 8494000002, Exp 7/31/28

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0767-2026
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedJuly 28, 2026
ReportedAugust 26, 2026
CompanyRegeneron Pharmaceuticals Inc
Company locationTarrytown, NY, United States
Initiated byVoluntary: Firm initiated
Quantity21,353 vials

More recalls from Regeneron Pharmaceuticals Inc · all drug recalls · recalls from July 2026

Official FDA record