FDA Enforcement Class II Terminated

CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US

Recall: Z-0939-2022 · Reported April 20, 2022

Enforcement

Recall Number
Z-0939-2022
Event ID
89810
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Graphic Controls Acquisition Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
April 20, 2022
Initiation Date
March 15, 2022
Classification Date
April 14, 2022
Termination Date
July 12, 2024
Address
400 Exchange St, N/A, Buffalo, NY, 14204-2064, United States

Description

CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780 50603-US

Reason

Instructions for Use (IFU) (Instructions for Use) indicate compliance with ANSI/AAMI EC53:2013/(R)2020 ECG trunk cables and patient leadwires. Section 5.3.9 of the standard requires the device to withstand, without breakdown , an application of, 5,000 V d.c. when used with a defibrillator at a voltage above its maximum threshold, Claravue does not meet the specification and delivers an inefficient electrical charge which may result in an ineffective defibrillation.

Code Info

All lots UDI: 03700506307319

Distribution

US Nationwide distribution in the States of AR, CA, CO, FL, IN, KS, MA, MN, NY, OK, VT.

Quantity

N/A