Philips Medical Systems, Inc. - Philips Healthcare - Class 2 Recall
Philips HeartStart MRx Monitor/Defibrillator Models:M3535A, M3536A, M3536M, M3536MC, M3536M4, M3536M5 The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 11, 2015 Category: Medical Equipment Source Type: alerts
Philips Medical Systems, Inc. - Philips Healthcare - Class 2 Recall
HeartStart MRx monitor/defibrillator Models M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 5, 2015 Category: Medical Equipment Source Type: alerts
Philips Electronics North America Corporation - Philips HeartStart - Class 2 Recall
Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation. When operating as a semi-automatic external defibrillator in AED Mode, the HeartStart XL+ is suitable for use by medical personnel trained in basic life support that includes the use of an AED. When operating in Monitor, Manual Defibrillation or Pacing modes, the HeartStart XL+ is suitable for use by healthcare professionals trained in advance...
Source: Medical Device Recalls - August 5, 2015 Category: Medical Equipment Source Type: alerts
GILLETTE CLINICAL ADVANCED TRAINING DAY (Aluminum Zirconium Trichlorohydrex Gly) Cream [Procter And Gamble Manufacturing Company]
Updated Date: Jun 15, 2015 EST (Source: DailyMed Drug Label Updates for the last seven days (since May 20, 2007 EST))
Source: DailyMed Drug Label Updates for the last seven days (since May 20, 2007 EST) - June 15, 2015 Category: Drugs & Pharmacology Source Type: alerts
Philips Medical Systems, Inc. - Philips MRx Defibrillator - Class 2 Recall
HeartStart MRx Monitor/Defibrillator; Model. Numbers: M3535A, M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 14, 2015 Category: Medical Equipment Source Type: alerts
Baxter Healthcare Corp. - HomeChoice/HomeChoice PRO - Class 2 Recall
HomeChoice Automated PD system and HomeChoice Pro Automated PD system Baxter's HomeChoice and HomeChoice Pro APD systems are designed to provide Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients. Their Fill volumes can range from 60 mL to 3000 mL. The HomeChoice and HomeChoice Pro APD systems are intended to be operated by: 1) Home patients whose physicians have prescribed this system. Patients, or their caregivers, must have received adequate training to use the system. 2) Clinicians who are using the system for patients under their care and under a prescription. Clinicians must ha...
Source: Medical Device Recalls - January 8, 2015 Category: Medical Equipment Source Type: alerts
Alere San Diego, Inc. - INRatio Monitors - Class 1 Recall
INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional - 0100007 INRatio Prothrombin Time (PT) Monitoring System - 0100137 Alere INRatio Replacement Monitor The test systems contain individually packaged components needed to use the product, such as a monitor, user guide, quick reference guide training DVD or CD, Lancets (home monitoring kits contain an Autolet, Unilet, gauze pads, and alcohol wipes), power supply (home monitoring kits contain AA batteries), results log book and a warranty card. None of the components, except for the lancets, are sterile. In vitro diagnostic monitoring system used fo...
Source: Medical Device Recalls - January 4, 2015 Category: Medical Equipment Source Type: alerts
Alere San Diego, Inc. - INRatio 2 Monitors - Class 1 Recall
INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Testing System - 0200432 Alere INRatio 2 PT/INR Home Monitoring System - 0200433 Alere INRatio 2 PT/INR Home Monitoring System - 0200457 Alere INRatio 2 Replacement Monitor - 55112 Alere INRatio 2 Replacement Monitor - 55131 Alere INRatio 2 Replacement Monitor - 55128A Alere INRatio 2 PT/INR Professional Monitoring System The test systems contain individually packaged components needed to use the product, such as a monitor, user guide, quick reference guide training DVD or CD, Lancets (home monitoring kits contain an Autolet, Unilet, gauze pads, and...
Source: Medical Device Recalls - January 4, 2015 Category: Medical Equipment Source Type: alerts
Philips Medical Systems, Inc. - Philips Healthcare - Class 2 Recall
Philips HeartStart XL+ Defibrillator/Monitor with system software version B.00.00 or B.00.01 installed Model: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation. When operating as a semi-automatic external defibrillator in AED Mode, the HeartStart XL+ is suitable for use by medical personnel trained in basic life support that includes the use of an AED. When operating in Monitor, Manual Defibrillation or Pacing modes, the HeartStart XL+ is suita...
Source: Medical Device Recalls - April 10, 2014 Category: Medical Equipment Source Type: alerts
Philips Medical Systems, Inc. - Philips Healthcare - Class 2 Recall
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation. When operating as a semi-automatic external defibrillator in AED Mode, the HeartStart XL+ is suitable for use by medical personnel trained in basic life support that includes the use of an AED. When operating in Monitor, Manual Defibrillation or Pacing modes, the HeartStart XL+ is suitable for use by healthcare professionals trained in ...
Source: Medical Device Recalls - April 10, 2014 Category: Medical Equipment Source Type: alerts
Philips Medical Systems North America Inc. - Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs) - Class 2 Recall
Philips HeartStart Home and OnSite (HS1) automated external defibrillators (AEDs). Product Usage: The models M5066A, M5067A, and M5068A are designed for use on a person in sudden cardiac arrest who is: -Unresponsive when shaken -Not breathing normally If in doubt, apply the pads. A training class in CPR/AED use is recommended for anyone who may use the HS1. If the person is an infant or child younger than eight years old or weighs less than 55 lbs (25 kg), use the special infant/child pads. If the child appears older/larger, use the adult pads. Do not delay treatment to determine the child s exact age or weight. If in...
Source: Medical Device Recalls - March 20, 2014 Category: Medical Equipment Source Type: alerts
Veridex, LLC - Janssen Diagnostics, LLC - Class 2 Recall
CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II¿ is a semi-automated fluorescence microscope, consisting of the analyzer, a dedicated computer with CELLTRACKS¿ software, monitor, keyboard, mouse and uninterruptible power supply (UPS). The system also supports an optional Remote Review Workstation (RRW), which consists of a dedicated computer with CELLTRACKS¿ software, monitor, keyboard and mouse. Use of this product requires training and should be used under the supervision of laboratory management. The CELLTRACKS ANALYZER II¿ is for analysis of rare cell...
Source: Medical Device Recalls - March 14, 2014 Category: Medical Equipment Source Type: alerts
Philips Medical Systems, Inc. - Phillips HeartStart MRx Monitor/Defribillator - Class 2 Recall
Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with Q-CPR Meter Option B08 The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 13, 2014 Category: Medical Equipment Source Type: alerts
Philips Medical Systems, Inc. - Philips Healthcare - Class 2 Recall
HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 27, 2014 Category: Medical Equipment Source Type: alerts
Philips Medical Systems, Inc. - HeartStart MRx Monitor/Defribillator - Class 2 Recall
M3536A HeartStart MRx with Wireless Link Upgrade (861289) The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac support, or defibrillation. It must be used by or on the order of a physician. (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 27, 2014 Category: Medical Equipment Source Type: alerts
