medical Class I Updated 2023-06-28

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls ICD COBALT XT HF QUAD OUS, Model Number DTPA2QQG; Implantab

Recalled Product

ICD COBALT XT HF QUAD OUS, Model Number DTPA2QQG; Implantable Cardioverter Defibrillators


Hazard / Issue

There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glassed) feedthrough, including currently available ICDs and CRT-Ds.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: GTIN 00763000501020, Lot Serial Numbers: RTC614024S, RTC617998S, RTC614026S, RTC617999S, RTC618002S, RTC618007S, RTC621332S, RTC614023S, RTC611661S
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