Medtronic Recalls Cardiac Defibrillators Due To Reduced Shock Potential

The device giant is recalling Cobalt and Crome defibrillators because they may deliver weaker shocks than intended.

Sign of Medtronic at Canada Headquarters in Brampton, Ontario, Canada.
• Source: Shutterstock

Medtronic plc announced on 11 August that it is recalling Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) over performance issues.

According to the company, the recalled cardiac implants may deliver reduced shock volume during high-voltage therapy due to a short-circuit protection event. Affected units may deliver only 79% of the programmed energy, which could make them 1% less effective

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