WhichRecall
Class IIReported 2025-09-10

KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion After Dilution, Single-Does vial. Mfd by: Immunocore Limited, 92 Park Drive, Abingdon, Oxfordshire, OX14 4RY, United Kingdom, For: Immunocore Commercial LLC, 181 Washington St, Conshohocken, PA, 19428, Product of Denmark NDC 80446-0401-01 Lot #: 3D009AA09, 3D009AA10, 3D009AA25, Exp Date: 31 MAR 2026 NDC 80446-0401-99 (Non-Commercial FG) Lot #: 3D009AA02, Exp Date 31 MAR 2026

Recalled by IMMUNOCORE, LLC

Reason for Recall

Subpotent Drug

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Recall Number
D-0614-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-06-10
Reported
2025-09-10
Distribution
US Nationwide
Code Info
NDC 80446-0401-01 Lot #: 3D009AA09, 3D009AA10, 3D009AA25, Exp Date: 31 MAR 2026 NDC 80446-0401-99 (Non-Commercial FG) Lot #: 3D009AA02, Exp Date 31 MAR 2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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