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October 18, 2016
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Warning About Faulty Defibrillators
02 February, 2021
Just in case you haven’t already seen the news reports about faulty defibrillators…
The Medicines and Healthcare Products Regulatory Agency (MHRA) has issued a Medical Device Alert for the LIFEPAK CR Plus or a LIFEPAK EXPRESS Automatic External Defibrillator (AED).
There is a reported electrical fault with some of the above models.
The fault is due to an internal component (reed switch) that can intermittently become stuck in the closed position. This could fail to deliver a shock to resuscitate a patient. There are around 2,577 devices reported as defective.
The Devices Faulty Defibrillators Affected
These devices are commonly known as public access defibrillators (PAD) because anyone can use them in an emergency. The manufacturer, Physio-Control, has sent a safety alert to people with affected defibrillators, with instructions on what to do. Whilst there have been no reported patient incidents, it is important that the manufacturer’s instructions are followed by completing and returning the confirmation sheet immediately.What To Do If You Own A Physio-Control Defibrillator:
- You need to check that the serial number listed in the confirmation sheet matches the serial number on the label located on the back of the device.
- When the on/off button is pressed and the lid is opened a voice prompt may fail to initiate.
- If voice prompts are not activated within 5 seconds, people should remove their device, not use it and contact the manufacturer’s customer support to arrange for the reed switch to be replaced.
- If the voice prompt is initiated within 5 seconds, people with affected defibrillators can still use them but should continue to monitor them in line with their routine check process until contacted by the manufacturer, Physio-Control, to arrange for the reed switch to be replaced.




