Lifepak20 Defibrillator Recalled
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Symposier - Recall of Certain LIFEPAK Defibrillators
symposier.com — “Uploaded and shared in Youtube by: USFoodandDrugAdmin " Physio-Control has alerted users of LIFEPAK 20 and LIFEPAK 20e defibrillators about possible failures in AC or DC power that could delay or prevent these devices from delivering therapy. If a failure occurs while the device is being used in the AC or line-power mode, the unit should automatically switch to the DC, or battery mode. But after the battery is depleted, the AC failure will prevent the battery from recharging and all power will b” View full resource at symposier.com
Most Recently Shared on October 1, 2010 at 6:57 pm By:
Symposier Cardiology Cardiology and Health Business
Recall of Certain LIFEPAK Defibrillators. http://bit.ly/9K2NHz #FDA
Physio-Control initiates field correction on certain LIFEPAK 20/20e defibrillator/monitors
news-medical.net — “Physio-Control, Inc., a wholly owned subsidiary of Medtronic, Inc.,, announced the company's recent initiation of a field correction on certain LIFEPAK 20/20e defibrillator/monitors manufactured prior to January 9, 2009. Analysis conducted by Physio-Control verified a possible battery (DC) power malfunction on the affected devices. In the malfunction scenario, a loss of battery power may occur while the unit is in operation.” View full resource at news-medical.net
Most Recently Shared on July 3, 2010 at 10:27 am By:
Physio-Control initiates field correction on certain LIFEPAK 20/20e defibrillator/monitors: Physio-Control, Inc., ... http://bit.ly/aAQPRb
Defibrillator Recall Advice
usrecallnews.com — “There are many manufacturers of Automated External Defibrillators (AEDs). Although the units must pass the same rigid FDA tests in order to be marketed to the public, when it comes to recalls, all units are not alike.” View full resource at usrecallnews.com
Most Recently Shared on January 12, 2010 at 2:12 am By:
New Recall Alert: : Defibrillator Recall Advice http://www.usrecallnews.com/2010/01/defibrillator-recall-advice.html
AED 10 and MRL Jumpstart Defibrillators Recalled
usrecallnews.com — “Over 14-Thousand external AED 10 and MRL JumpStart defibrillators have been recalled after 39 reports of incidents, including two deaths.” View full resource at usrecallnews.com
Most Recently Shared on March 12, 2009 at 6:43 pm By:
New blog post: AED 10 and MRL Jumpstart Defibrillators Recalled http://tinyurl.com/cwr38x
Medtronic subsidiary hit with defibrillator recall « MedCity News
medcitynews.com — “Medtronic subsidiary hit with defibrillator recall « MedCity News” View full resource at medcitynews.com
Most Recently Shared on July 7, 2010 at 7:21 pm By:
Medtronic subsidiary hit with defibrillator recall http://bit.ly/cbbYcR
Defibtech Recalls DDU-100 series AEDs: Automatic External Defibrillators (AED)
usrecallnews.com — “Defibtech, LLC has recalled about 65,885 DDU-100 series semi-automatic external defibrillators (AEDs) sold in the United States under the brand names Lifeline AED and ReviveR AED. These recalled defibrillators may, in rare cases, cancel shock while charging, which could cause a failure to resuscitate the patient.” View full resource at usrecallnews.com
Most Recently Shared on May 4, 2011 at 10:33 pm By:
Defibtech Recalls DDU-100 series AEDs: Automatic External Defibrillators (AED) http://p.ost.im/p/7aeNw
Philips Issues Worldwide Recall of Select Heartstart Fr2+ Automated External Defibrillators
fda.gov — “Philips announced today that it is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs). This recall is being conducted due to the possibility of a memory chip failure that may render the device inoperable. Only certain HeartStart FR2+ AEDs (models M3860A and M3861A, distributed by Philips; and models M3840A and M3841A, distributed by Laerdal Medical) manufactured between May, 2007 and January, 2008 are included in the voluntary recall.” View full resource at fda.gov
Most Recently Shared on October 3, 2009 at 12:55 pm By:
Physician Assistants Health News Feed
Recall: 5,400 HeartStart FR2+ automated external defibrillators (AEDs) with bad memory chips: http://tinyurl.com/yevnons
FDA Panel Recommends Tougher Standards for External Defibrillators
health.yahoo.net — “TUESDAY, Jan. 25 (HealthDay News) -- Following a series of recalls of external defibrillators, a U.S. Food and Drug Administration panel of experts recommended Tuesday that the devices be held to stricter standards.” View full resource at health.yahoo.net
Most Recently Shared on January 26, 2011 at 1:03 pm By:
Jane Anderson Healthy Eating Advisor
FDA Panel Recommends Tougher Standards for External Defibrillators http://bit.ly/gpysE6
FDA Panel Recommends Tougher Standards for External Defibrillators
health.yahoo.net — “TUESDAY, Jan. 25 (HealthDay News) -- Following a series of recalls of external defibrillators, a U.S. Food and Drug Administration panel of experts recommended Tuesday that the devices be held to stricter standards.” View full resource at health.yahoo.net
Most Recently Shared on January 26, 2011 at 12:57 pm By:
Jennifer Ann Grisso Nurse and Active Health Library
FDA Panel Recommends Tougher Standards for External Defibrillators: TUESDAY, Jan. 25 (HealthDay News) -- Follow... http://bit.ly/gBpILp
Recall of Cardiac Science AEDs
theheart.org — “The safety alert affects approximately 280000 devices made by Cardiac Science Corporation, the primary dysfunction being a failure to deliver a shock during the resuscitation attempt.” View full resource at theheart.org
Most Recently Shared on April 28, 2010 at 3:21 pm By:
Updated recall of 14 Cardiac Science automated defibrillators: The safety alert affects approximately 280Â 000 devi... http://bit.ly/duQN31
Cardiac Science Corp. to replace defibrillators part of 2009 recall « MedCity News
medcitynews.com — “Cardiac Science Corp. to replace defibrillators part of 2009 recall « MedCity News” View full resource at medcitynews.com
Most Recently Shared on July 19, 2010 at 9:33 pm By:
Cardiac Science Corp. to replace defibrillators part of 2009 recall http://bit.ly/bhALU1
FDA Classifies Riata and Riata ST Silicone Defibrillation Leads as Class I Recall
usrecallnews.com — “The FDA has classified this recall as a Class I recall because of the potential risk of serious injury or patient death if affected devices malfunction.” View full resource at usrecallnews.com
Most Recently Shared on December 19, 2011 at 7:10 pm By:
FDA Classifies Riata and Riata ST Silicone Defibrillation Leads as Class I Recall http://t.co/SVKRv2mh
Dorset man saved by defibrillator recalls his experience - Minden Times - Ontario, CA
mindentimes.ca — “He was playing volleyball when it happened. It was a typical Thursday night near the end of February with Paul Whitelaw trying to get a little...” View full resource at mindentimes.ca
Most Recently Shared on March 7, 2012 at 2:55 pm By:
Heart and Stroke FDN Health Organization
AEDs in recreational facilities save lives. Man saved by defibrillator recalls his experience: http://t.co/nfrI92id
Fix heart defibrillators, FDA tells manufacturers - latimes.com
latimes.com — “Heart defibrillators often used in cardiac arrests outside hospitals can have harmful shortcomings that must be fixed, the Food and Drug Administration says. It cites rising numbers of failures and recalls but says the devices' lifesaving potential still outweighs the risks.” View full resource at latimes.com
Most Recently Shared on November 15, 2010 at 11:57 pm By:
Fix heart defibrillator problems, FDA tells manufacturers http://lat.ms/cvjCTX
Medicine and Technology [part of HCPLive]: FDA launches the External Defibrillator Improvement Initiative
medicineandtechnology.com — “Medicine and Technology [part of HCPLive]: FDA launches the External Defibrillator Improvement Initiative” View full resource at medicineandtechnology.com
Most Recently Shared on November 16, 2010 at 2:00 pm By:
Joseph Kim, MD, MPH Doctor and Physician
FDA launches the External Defibrillator Improvement Initiative http://goo.gl/fb/WaZV8
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