Skip to content
Recall Observatory FDA recall evidence

Device product

PARADYM Models: VR 8250, DR 8550, CRT-D 8750, RF VR 9250, RF DR 9550, RF CRT-D 9750, SonR 8770, RF SonR 9770 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.

Z-2113-2017

April 11, 2017

Class II

Product summary

Firm
Sorin Group Italia SRL - CRF
Event
Event 77139
Status
Terminated
Classification
Class II
Quantity
4700
Official record key
device-enforcement:Z-2113-2017

Official wording

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

Code information: Product Code: ICV1199, ICV1200, ICV1179, TDF011U, TDF010U, TDF012U

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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

Field note

Send feedback

We'll only use this to respond to your feedback.