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AED Manufacturer's Bulletins
- Medical Device Recall: LifePak CR Plus Automated External Defibrillators: The product was recalled because the AED instructs the responder by voice prompts to press the shock button which is not visible because it is covered, thereby making the responder unable to provide shock therapy. The AED device should be removed from service, or the manufacturer-provided diagram should be consulted to remove and discard the shock button cover.
Link to the Website September 11, 2008
- LifePak CR Plus Automated External Defibrillators (Physio-Control, Inc) Recall: FDA notified healthcare professionals of a Class I recall of certain LIFEPAK CR Plus Automated External Defibrillators (AED) manufactured and distributed from July 9, 2008 through August 19, 2008. An extremely humid environment may cause the affected devices to improperly analyze the heart rhythm and may cause the device to delay or fail to deliver therapy.
Link to the Website September 18, 2009
Link to all AED Recalls September 22, 2009
