Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraopera...

FDA Recall #Z-1466-2025 — Class II — February 24, 2025

Recall #Z-1466-2025 Date: February 24, 2025 Classification: Class II Status: Ongoing

Product Description

Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint Guardian Intraoperative Lead, Small Model/Catalog Number: REF# 9524 (Small) Product Description: The Checkpoint Guardian Intraoperative Leads are single-patient disposable accessories for providing stimulus to a targeted nerve. The accessories are intended for use with any device from the Checkpoint Stimulator/Locator Family. The lead electrode is intended to wrap around nerves that have been surgically exposed, allowing the surgeons to provide hands free stimulus to a targeted nerve.

Reason for Recall

Adhesive on the back of the lead may not fully encapsulate the metallic portion of the wire and button subassembly, potentially leading to exposed metal. There is a risk of electrical current leakage, which may lead to inconsistent or confusing muscle responses, potentially compromising the effectiveness of the intended use as the surgeon could take an incorrect clinical action.

Recalling Firm

Checkpoint Surgical Inc — Cleveland, OH

Classification

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

Product Type

Devices

Product Quantity

135

Distribution

US Nationwide distribution.

Code Information

UDI-DI B13095240 Small Lot 4318 Expires 01Apr2026 Lot 4325 Expires 01Apr2026 Lot 4368 Expires 01Dec2026

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated