List of FDA Device Recalls 2010
Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED® and ReviveR AEDTM
ZOLL E Series Defibrillator/Pacemaker/Monitors
Philips—CPR Meters Used with HeartStart MRx Monitors/Defibrillators
Cardiac Science Notifies AED Customers of Voluntary Medical Device Recall
PediCap™ End-Tidal CO2 Detectors Recall
Stryker Medical Chair Recall
Welch Allyn AED 10 Recall
Kidde XL Recall
Zoll AED Plus Defibrillator May Not Deliver Defibrillation Shock
Smiths Medical Issues Urgent Device Recall Of Portex® Pediatric-Sized Tracheal Tubes
Covidien Pedi-Cap End-Tidal CO2 Detector
Physio-Control Inc., LIFEPAK CR Plus AEDs Recall Class: Class I Date Recall
Philips Issues Worldwide Recall of Select Heartstart Fr2+ AED's
Cardiac Science Notifies AED Customers of Nationwide Voluntary Medical Device Correction
ConvaTec doing business as Unomedical, Inc., Manual Pulmonary Resuscitator (MPR) (Single-Patient Use)
LifeScan, Inc. is conducting a voluntary recall of eight lots of OneTouch® SureStep® Test Strips
