Recall Issued for St. Jude Medical Cardiac Defibrillator Devices
Defective batteries are at the root of a recall issued by the FDA for implantable cardioverter defibrillators (ICD) and cardiac resynchronization therapy defibrillators (CRT-D) manufactured by St. Jude Medical, Inc. The recalled devices include the Fortify, Unify, and Quadra models of ICDs and CRT-Ds. The recall was issued after a defect was identified that could cause the lithium-ion batteries to short circuit and fail prematurely putting the patient’s life at risk.
Two deaths have been reported due to a defective battery that did not give the life-saving pacing or shocks necessary. Another 50 patients have reported dizziness and fainting due to defective batteries that failed to deliver the needed pacing therapy.
If you or someone you know has a recalled St. Jude Medical cardiac defibrillator device and has suffered an injury, contact us. Our product liability attorneys have litigated thousands of claims on behalf injured people against large medical device makers like St. Jude Medical. We can provide you with a free case evaluation and advise you of your legal rights and options.
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