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 The leading web portal for pharmacy resources, news, education and careers November 19, 2017
Pharmacy Choice - Pharmaceutical News - Faulty Defibrillator: Users Urged to Check Battery Connection - November 19, 2017

Pharmacy News Article

 5/19/17 - Faulty Defibrillator: Users Urged to Check Battery Connection

LONDON, May 18 The British Medicines and Healthcare Products Regulatory Agency issued the following news release:

People and organisations should check public access defibrillators for a technical fault, the Medicines and Healthcare products Regulatory Agency advised today.

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 manufacturer, Physio-Control, has sent a safety alert to people with affected defibrillators with instructions for action. If you have not received an FSN from the manufacturer, please contact them directly. The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a Medical Device Alert.

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.

It is important that the manufacturer's instructions are followed by completing and returning the confirmation sheet immediately.

People should check that the serial number listed in their confirmation sheet matches the serial number on the label located on the back of the device.

If your device powers off unexpectedly, either during inspection or during patient treatment, immediately remove and reinstall your existing battery to restore power to the device. If power is not restored, replace the battery with a spare battery and call Physio-Control immediately to arrange for servicing of your device.

It is important to implement a weekly schedule of battery removal and reinstallation for all LIFEPAK 1000 devices until contacted by PhysioControl to arrange repair for any affected devices. Removing and reinstalling the battery on a weekly basis will help make sure your device is ready for use. It is also important to always carry a fully charged spare battery.

As part of the maintenance and testing schedule, users of the LIFEPAK 1000 Defibrillator should always follow the Operating Instructions which direct users to routinely inspect both the battery well and battery contacts, especially if the devices have been exposed to vibrations or the battery has been installed for an extended period without being removed.

John Wilkinson, MHRA's Director of Medical Devices said:

* These devices deliver life-saving treatment and it is vital they operate correctly when needed in an emergency.

* People who are responsible for them should carry out the checks recommended by the manufacturer.

* If you have any questions please contact Physio-Control on 0808 258 0094.



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