A formal notification issued by a device manufacturer when a potential safety issue is identified with a specific model of ICD, pacemaker, or leads. An advisory (sometimes called a safety alert or field safety corrective action) does not always mean the device needs to be replaced — many advisories result in a change to programming or increased monitoring. Patients affected are contacted by their device clinic, who will advise on any recommended action. If you are concerned about whether your device is subject to an advisory, contact your clinic.
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