Sunitinib Malate Capsules, 25 mg, 28-count bottles, Rx Only, Manufactured for: AvKARE, Pulaski, T...

FDA Recall #D-0104-2025 — Class II — October 18, 2024

Recall #D-0104-2025 Date: October 18, 2024 Classification: Class II Status: Ongoing

Product Description

Sunitinib Malate Capsules, 25 mg, 28-count bottles, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 42291-902-28

Reason for Recall

Labeling: Label Mix-Up

Recalling Firm

AvKARE — Pulaski, TN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

20 bottles

Distribution

Nationwide within the United States

Code Information

Lot #: 100049501, Exp. Date 07/31/2026

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated