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Medtronic Recalls ICDs and CRT-Ds for Risk of Low or No Energy Output During High Voltage Therapy

Medtronic is recalling all ICDs and CRT-Ds, manufactured after 2017, with a glassed feedthrough as they may deliver low or no energy output when needed for high voltage therapy.

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Medtronic announces Class I recall for certain implantable defibrillators

Due to a risk of low or no energy output during high voltage therapy, Medtronic and the FDA announced a Class I recall of certain Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) with Glassed Feedthrough.

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Class I Recall for 350,000 Medtronic Defibrillators: FDA

The agency says affected devices may deliver a low-energy shock, or none at all, in patients who need it.

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Medtronic recalls certain implantable cardiac defibrillators

The FDA designated a recall of some Medtronic (NYSE: MDT) defibrillators as Class I, the most serious kind.

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Medtronic Recalls Cobalt XT, Cobalt and Crome ICDs and CRT-Ds for Risk that Devices May Issue a Short Circuit Alert and Deliver Reduced Energy Shock During High Voltage Therapy

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

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