MHRA_Faulty defibrillator: users urged to check battery connection
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MHRA_Faulty defibrillator: users urged to check battery connection
From: Medicines and Healthcare products Regulatory Agency
Published:18 May 2017
People and organisations should check if they have the defibrillator model, LIFEPAK 1000 Automatic External Defibrillators (AED), because a technical fault with some of them means they may not deliver an electric shock to the heart to someone who is in cardiac arrest.
This issue could potentially affect all LIFEPAK 1000 devices. There are 10,068 devices in the UK.
These devices are available in public places such as schools, airports, football stadiums and leisure centres. They are often known as public access defibrillators (PAD) as they are intended to be used by anyone. They are also found in hospitals, clinics and ambulances. The manufacturer’s logo on the front cover may vary, displaying ‘Medtronic’ or ‘Physio-Control’.
The fault is due to intermittent connection between the battery and device contacts because of wear and subsequent corrosion between both components. This could fail to deliver a shock to resuscitate a patient."
https://www.gov.uk/government/news/faul ... connection
Links to manufacturer on webpage with required actions
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