ClearanceBrief
Recall Z-1417-2017 ยท MKJ Automated External Defibrillators (Non-Wearable)

Philips North America, LLC

HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9

DateMar 24, 2017 (initiated Feb 24, 2017)
StatusTerminated
ReasonHeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when operating using a single battery as the sole source of power may fail to deliver therapy or monitoring
Root causeDevice Design
ActionPhilips Healthcare issued an Urgent Medical Device Correction notification/Field Safety Notice. on 2/24/17. The Urgent Medical Device Correction notification/ Field Safety Notice informs customers of the issue, identifies details of the units affected, gives instructions on actions to be taken by the customer and identifies what action Philips plans to take to remedy the issue. Action (1) Philips is voluntarily initiating this correction and is providing Instructions for Use (IFU) Addendum titled, HeartStart MRx Battery Connector Pins for all customers with affected units. Philips is asking
Quantity97,794 total ( 47,362 US and 50,429 OUS)
DistributionWorldwide Distribution-US (Nationwide) including PUERTO RICO and countries of: AFGHANISTAN, ALBANIA, ANGOLA, ARGENTINA, ARUBA, AUSTRALIA,AUSTRIA,AZERBAIJAN,BAHRAIN, BANGLADESH, BELGIUM, BOLIVIA,BOSNIA AND HERZEGOWINA, BRAZIL,BRUNEI DARUSSALAM, BULGARIA,CAMBODIA,CANADA,CHILE,CHINA,COLOMBIA,COSTA RICA
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K031187HEARTSTART MRX, MODEL M3535A
Philips Medical Systems, Aug 27, 2003
K040404HEARTSTART MRX, MODEL M3535A
Philips Medical Systems, Inc., May 4, 2004
K051134HEARTSTART MRX WITH Q-CPR OPTION, MODELS M3535A OR M3536A
Philips Medical Systems, Sep 8, 2005
K061707HEARTSTART MRX, INVASIVE PRESSURE & TEMPERATURE OPTIONS
Philips Medical Systems, Aug 11, 2006
K062233HEARTSTART MRX MONITOR/DEFIBRILLATOR
Philips Medical Systems North America, Inc., Nov 22, 2006