device recall
saveMedtronic, Inc. device recall (Cls II)
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Aurora EV-ICD and Clinical EV-ICD, single chamber, extravascular implantable cardioverter defibrillators (ICD), Product Number DVEA3E4 — Reason: There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur. — Status: Ongoing
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