Z-2114-2017 Class II Terminated

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

Recall Details

Product Type
Devices
Report Date
May 24, 2017
Initiation Date
April 11, 2017
Termination Date
May 22, 2020
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
37

Product Description

INTENSIA Models: VR 124, DR 154, CRT-D 174 Product Usage: OVATIO VR 6250, OVATIO DR 6550, PARADYM VR 8250, PARADYM DR 8550, PARADYM RF VR 9250, PARADYM RF DR 9550, INTENSIA VR 124 and INTENSIA DR 154 are 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). OVATIO CRT 6750, PARADYM CRT-D 8750, PARADYM SonR 8770, PARADYM RF CRT-D 9750, PARADYM RF SonR 9770 and INTENSIA CRT-D 174 are indicated for ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life threatening arrhythmias. The devices are also indicated for the reduction of heart failure symptoms in medically optimized NYHA Functional Class III and IV patients with left ventricular ejection fraction of 35% or less, and a QRS duration of 150 ms or longer.

Reason for Recall

Sorin is notifying physicians that certain defibrillators' battery depletion may be undetectable.

Distribution Pattern

US Nationwide Distribution

Code Information

Product Code: TDF022C, TDF021C, TDF020C