US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Sep 23, 2024 (2 years ago)

Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP deviations

What was recalled

Pluvicto, 1000 MBq/mL (27 mCi/mL), lutetium, LU 177, vipivotide tetraxetan injection, Single-dose vial, Sterile, Manufacturer Advanced Accelerator Applications, 57 E. Willow Street, NJ 07041, Millburn USA. NDC 69488-0010-61

Recalling firm
Advanced Accelerator Applications USA, Inc.
NDC code
69488-0010-61
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0007-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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