defibrillators

Hacking Risk Sparks 465k St. Jude Pacemakers to be Recalled

Hacking Risk Sparks 465,000 St. Jude Pacemakers Recall

Patients vulnerable to a software glitch The U.S. Food and Drug Administration (FDA) is warning that over 465,000 patients who had St. Jude pacemakers implanted may be vulnerable to a [...]

FDA Issues Warning On Durata and Riata ST Optim

St. Jude Defibrillators May Be Linked To Serious Cardiac Side Effects

Parker Waichman LLP is investigating potential lawsuits on behalf of individuals who were implanted with potentially defective St. Jude defibrillators and leads that may cause serious side effects, including cardiac [...]

St. Jude Medical ICD and CRT-D Defibrillators Recall

St. Jude Medical Implantable Cardioverter Defibrillators Subject of Recall Following Deaths. Jude Medical Inc. recently announced a recall of about 40 implanted heart devices over risks of premature battery depletion. The [...]

Investigation of St. Jude Medical Devices Now Includes FDA

The U.S. Food and Drug Administration (FDA) has now joined the investigation into security claims that devices made by St. Jude Medical can be hacked remotely. These claims are still [...]

St. Jude Medical Recalls Defibrillator Leads Due to Damaged Insulation

On January 22, 2016, device maker St. Jude Medical announced that a voluntary global field safety action related for the company’s Optisure Dual Coil Defibrillation Leads has now been designated [...]

Fda Clears Remaining Recalled Boston Scientific Defibrillators

Remaining Recalled Boston Scientific Defibrillators Cleared by FDA

Recalled Boston Scientific Defibrillators. Boston Scientific has resumed sales of five defibrillators that had been the subject of a recall several months ago. In a regulatory filing, the company said [...]

LIFEPAK 15 Monitor/Defibrillators Recall

LIFEPAK 15 Monitor/Defibrillators. LIFEPAK 15 monitor/defibrillators manufactured by Medtronic Inc.’s Physio-Control Unit have been named in a Class I recall. The LIFEPAK 15 monitor/defibrillator is designed for use by trained [...]

Boston Scientific Defibrillators Pose Dangers

Defibrillators May Cause Life-Threatening Shocks. Boston Scientific Corp.’s Cognis and Teligen brand defibrillators have a design flaw that can cause them to deliver unneeded, painful, and life-threatening shocks, according to [...]

Philips Healthcare Recalls Defibrillators

Recalled Defibrillators Approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs) are being recalled by Philips Healthcare. According to the recall notice, a potential memory chip failure may render the device [...]

Medtronic Recalls Defibrillators

Physio-Control, Inc., a division of Medtronic, Inc., is recalling LifePak CR Plus Automated External Defibrillators (AED). The Food & Drug Administration (FDA) has deemed this a Class I recall. This recalled device [...]

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4 years ago

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