International Medical Devices Database

Source
MHRA
1 Event
- Safety Alert Or Field Safety Notices for LIFEPAK 20/20e defibrillator/monitor

One device in the database

LIFEPAK 20/20e defibrillator/monitor

Model / Serial
Product Description
LIFEPAK 20/20e defibrillator/monitor. Specific serial numbers are affected. This is an acute cardiac care device used in clinical and hospital settings. It has a dual power supply system and is designed to operate on AC (mains) power or DC (battery) power. Devices with specific serial numbers, manufactured from 31 July 2002 to 9 February 2009 inclusive, are affected. See the manufacturer’s Field Safety Notice for a list of the relevant serial numbers.

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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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Medtronic/Physio-Control

One device in the database

LIFEPAK 20/20e defibrillator/monitor