Z-3232-2017 Class II Terminated

Recalled by Sorin Group Italia SRL - CRF — Saluggia, VC, N/A

Recall Details

Product Type
Devices
Report Date
October 4, 2017
Initiation Date
July 24, 2017
Termination Date
January 29, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
86 units

Product Description

Platinium DR DF4 1540, Model Number TDF036U, UDI/GTIN 08031527015477, Implantable cardioverter defibrillator, Biventricular or ventricular antitachycardia pacing, Dual or single chamber arrhythmia detection Product Usage: PLATINIUM VR is indicated for use in patients who are at high risk of sudden cardiac death due to ventricular tachyarrhythmias and who have experienced one of the following situations: - Survival of at least one episode of cardiac arrest (manifested by the loss of consciousness) due to ventricular tachyarrhythmia, - Recurrent, poorly tolerated sustained ventricular tachycardia (VT).

Reason for Recall

There is a possibility of overconsumption of certain PLATINIUM Implantable Cardiac Defibrillators (ICDs) and Cardiac ResynchronizationTherapy Defibrillators (CRT-Ds) following an ElectroStatic Discharge (ESD) during the implant surgery or a Magnetic Resonance Imaging (MRI) scan, and what actions to take.

Distribution Pattern

US Nationwide Distribution

Code Information

All Serial Numbers