BEUDAMED
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    Sertera Biopsy Device, Sterile; Used primarily in ultrasound-guided breast biopsies.

    FDA Recall
    Terminated ·Hologic, Inc·Product code KNW·August 22, 2016

    SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices. For uterine sound

    FDA Recall
    Terminated ·Hologic, Inc·Product code HHM·October 28, 2016

    Crimson Trace Corporation laser sights. The Finished Products are laser sighting systems for firearms, used for personal defense and target acquisition.

    FDA Recall
    Terminated ·Crimson Trace Corporation·Product code REU·October 10, 2017

    LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indicated for use on patients in cardiac arrest.

    FDA Recall
    Terminated ·Physio-Control, Inc.·Product code MKJ·May 9, 2014

    Physio-Control Lifepak 20 defibrillator/monitor is intended for the termination of certain fatal arrhythmias.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·June 18, 2008

    LIFEPAK Express Automated External Defibrillator (AED). Labeling on the device states LIFEPAK CR Plus/LIFEPAK EXPRESS Defibrillators with ADAPTIV Biphasic Technology; Medtronic Emergency Response Systems, Inc. 11811 Willows Road NE Redmond, WA. The battery operated, small portable device is primarily deployed in Public Access Defibrillator (PAD) environments where the expected use for any one device is once every 20 months. Product is capable of 30 full discharges. LIFEPAK Express AEDs are intended for use on victims/patients in cardiac arrest. It includes a patented shock advisory system that notifies the user (i.e. minimally trained responder) if it detects a cardiac rhythm that requires a shock. The individual must be unresponsive (unconscious), not breathing normally, and showing no signs of circulation (for example, no pulse, no coughing, or no movement). With Infant/Child Reduced Energy Defibrillation Electrodes, the LIFEPAK Express AEDs may be used on children who are up to 8 years old or who weigh up to 25kg (55 lb). The device is designed specifically for infrequent use and for use by people whose only training is in CPR and in using AEDs.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·July 24, 2008

    LIFEPAK CR Plus Automated External Defibrillator (AED). Labeling on the device states LIFEPAK CR Plus/LIFEPAK EXPRESS Defibrillators with ADAPTIV Biphasic Technology; Medtronic Emergency Response Systems, Inc. 11811 Willows Road NE Redmond, WA. The battery operated, small portable device is primarily deployed in Public Access Defibrillator (PAD) environments where the expected use for any one device is once every 20 months. Product is capable of 30 full discharges. LIFEPAK CR Plus AEDs are intended for use on victims/patients in cardiac arrest. It includes a patented shock advisory system that notifies the user (i.e. minimally trained responder) if it detects a cardiac rhythm that requires a shock. The individual must be unresponsive (unconscious), not breathing normally, and showing no signs of circulation (for example, no pulse, no coughing, or no movement). With Infant/Child Reduced Energy Defibrillation Electrodes, the LIFEPAK CR Plus AEDs may be used on children who are up to 8 years old or who weigh up to 25kg (55 lb). The device is designed specifically for infrequent use and for use by people whose only training is in CPR and in using AEDs.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·July 24, 2008

    Medtronic Physio-Control LIFEPAK CR Plus Defibrillator/Monitor. Automated external defibrillator deployed primarily in public access defibrillator environments where the expected use for any one device is once every 20 months. For use on persons requiring defibrillation therapy.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·July 31, 2009

    Physio-Control LIFEPAK 20e defibrillator/monitor. This product is an external defibrillator sold internationally only

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code LDD·May 13, 2008

    Physio-Control LIFEPAK 20 defibrillator/monitor. This product is an external defibrillator sold internationally and domestically.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code LDD·May 13, 2008

    LIFEPAK 20 defibrillator/monitor. Product Part numbers: 3202487-xxx, 3202488-xxx, U3202487-000, 3202488-015, and U3202488-000.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·May 27, 2010

    The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·February 8, 2013

    Keypad replacement for LIFEPAK20 or LIFEPAK20e. This product is an external defibrillator.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code LDD·May 13, 2008

    Internal Defibrillation Electrodes: PN: 805355-10 thru 14 and 805355-020 thru -024.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code LDD·January 29, 2008

    Biphasic LIFEPAK 15 Monitor/Defibrillator. The LIFEPAK 15 is a battery operated monitor with an external portable defibrillator used by healthcare providers in EMS, hospital and clinic settings. It operates in a manual or semi-automatic defibrillation mode and is offered with optional monitoring functions including Non-Invasive Blood Pressure (NIBP). When clinically indicated the LIFEPAK 15 allows the operator to deliver a brief, high energy, external shock through the chest to a patient's heart.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code DXN·August 12, 2009

    Biphasic LIFEPAK 15 Monitor/Defibrillator. Manufactured by Physio-Control Inc., a division of Medtronic, Inc. Redmond, Washington USA. The LIFEPAK 15 monitor/defibrillator is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient protocols.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·March 4, 2010

    The LIFEPAK 500 Automated External Defibrillator is a semi-automatic defibrillator that uses a patented Shock Advisory System. This software algorithm analyzes the patient's electrocardiographic (ECG) rhythm and indicates whether or not it detects a shockable rhythm. The LIFEPAK 500 AED is intended for use by personnel who are authorized by a physician/medical director and is intended for use in the pre-hospital and workplace and community environments.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code MKJ·June 12, 2013

    Physio-Control Internal Defibrillator Handles. PN: 3010901-002 for use with LIFEPAK 12 and 20. PN: 805249-014 thru 019 for use with LIFEPAK 9 and 9P.

    FDA Recall
    Terminated ·Physio Control, Inc.·Product code LDD·January 29, 2008

    Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments

    FDA Recall
    Terminated ·Carl Zeiss Meditec AG Rudolf-Eber-Str. 11 Oberkochen Germany·Product code JAD·August 30, 2017

    McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.

    FDA Recall
    Terminated ·MCKESSON TECHNOLOGIES INC.·Product code BSZ·March 15, 2013