AED Recalls

Extend the life of your AED as much as possible through our comprehensive database of AED recalls and updates available (most of which are free).

Don’t let your AED become out of date from American Heart Association (AHA) guidelines. AEDs are designed to be updated. Also, all major AED manufacturers and their models have had software or hardware upgrades through FDA field corrective actions or FDA equipment recall notices. Extend the life of your AED as much as possible through our comprehensive database of AED recalls and updates available (most of which are free).

Physio Control Medtronic / LIFEPAK 1000 Defibrillator Reported Instances of Device Shutting Down Unexpectedly During Patient Treatment

http://pikaiapilates.com/events/pilates-reformer-wednesday-am/ Recall Date: 01/13/2017
revengefully Title: LIFEPAK 1000 defibrillator due to reported instances where the device has shut down unexpectedly during patient treatment.
http://wendykeithdesigns.co.uk/wkd-featured-in-cornwall-today-magazine-i131.html Units: Lifepak 1000
buy gabapentin usa Issue: LIFEPAK 1000 defibrillator due to reported instances where the device has shut down unexpectedly during patient treatment.
Fix: Customers are also being advised to implement a weekly schedule of battery removal and reinstallation for all LIFEPAK 1000 devices. The removal and reinstallation of the battery will clean the contacts of oxidation and will reduce the likelihood of this issue from occurring. Physio-Control will be initiating a hardware device correction for all affected LIFEPAK 1000 devices and the company will contact customers to schedule device corrections once the hardware correction is ready for implementation. The company will provide customers with updated information regarding the timing for this device correction at the website URL shown below, when it is available.
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