FDA Recall Terminated

LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been validated for compatibility.

Recall: Z-1660-2008 · Initiated December 13, 2007

Recall

Recall Number
Z-1660-2008
Event Number
47336
Firm
Lifesync Corporation
FEI Number
1000403400
Product Code
DRG
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
December 13, 2007
Posted
September 16, 2008
Terminated
October 1, 2008
Address
One E. Broward Blvd., Suite 1701, Ft Lauderdale, FL, 33301

Description

LS-202 Large LeadWear Combo Pack - Disposable ECG Monitoring component intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been validated for compatibility.

Reason

LifeSync Wireless ECG System - Intermittent failure when using LS-202 and LS-232 LeadWear in conjunction with LS-41245 and LS-41285 Adaptors. The out of box failure manifests as a V-Lead failure, intended for use as a radiofrequency signal transmitter and receiver of electrocardiograph physiological signals which are displayed on the ECG monitors of various manufacturers' systems that have been

Action

Firm issued a Device Recall Letter on 12/14/2007. Users were requested to remove the product from inventory and discontinue use of the Large Sized LeadWear with the 12 Lead Adaptors. The current stock of product in inventory will be held under a stop shipment, pending destruction of non-conforming product.

Distribution

Class II Recall - Nationwide Distribution.

Quantity

576 completed leadwire units