ClearanceBrief
Recall Z-0208-2012 ยท DXH Transmitters And Receivers, Electrocardiograph, Telephone

Lifewatch Services Inc

ACT Cellular Phone Monitor; a component of the ACT Ambulatory Cardiac Telemetry; an automatically activated system with a high performance EKG, office hookup and auto send/auto detect that requires no patient intervention to either capture or transmit an arrhythmia when it occurs; Manufactured by Card Guard, 2 Pekeris St, Rehovot, 76100, Israel; there are two models used with either the ACT 1 sens

DateNov 17, 2011 (initiated Sep 26, 2011)
StatusTerminated
ReasonLifeWatch received complaints of minor shocks and burns during use of the LifeStar ACT systems with shorts in the leads.
Root causeNonconforming Material/Component
ActionThe firm, LifeWatch, sent an " Urgent Device Recall" letter dated September 27, 2011 to the affected customers. The letter describes the product, problem and action to be taken. The customers were instructed to immediately refrain from providing these devices to their customers; stop using the affected sensors, return their entire kit in the pre-paid mailer, and use the new device kit included with the recall letter. In addition, the letter informed the users that the replacement device has upgraded software and firmware that allows for detection of shorts in the cable, and if detected, cuts
Quantity532 phone monitors
DistributionNationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K071995CG-6108 CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR
Card Guard Scientific Survival , Ltd., Dec 18, 2007
K081257CG-6108 ACT-3L CONTINUOUS ECG MONITOR & ARRHYTHMIA DETECTOR
Card Guard Scientific Survival , Ltd., May 29, 2008
K101639CG-6108 ACT-IL CONTINUOUS ECG MONITOR AND ARRYTHMIA DETECTOR
Card Guard Scientific Survival , Ltd., Jun 25, 2010
K110499CG-5108 ACT-3L CONTINUOUS ECG MONITOR AND ARRHYTHMIA DETECTOR
Card Guard Scientific Survival , Ltd., Apr 6, 2011