Medtronic's Cardiac Rhythm and Heart Failure (CRHF) devices are designed to monitor and manage heart health. These devices help detect and treat arrhythmias, heart failure, and other cardiac conditions.
There is the potential for reduced shock energy (~79% of programmed energy) during high-voltage (HV) therapy for Cobalt and Crome implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds).
Medtronic's Cardiac Rhythm and Heart Failure (CRHF) devices are designed to monitor and manage heart health. These devices help detect and treat arrhythmias, heart failure, and other cardiac conditions.
These devices are medical devices designed for patient safety and require proper use to prevent complications.
Patients with cardiac conditions, including arrhythmias and heart failure
Ensure the device is used as directed by a healthcare professional, and that it is compatible with the patient's specific condition.
Consult with a healthcare professional to determine if the device is appropriate for your condition.
Follow the manufacturer's instructions for use and maintenance.
Regularly monitor device performance and report any issues to your healthcare provider.
Medtronic's Cardiac Rhythm and Heart Failure (CRHF) devices are medical devices designed to monitor and manage heart health. They help detect and treat arrhythmias, heart failure, and other cardiac conditions.
These devices use advanced technology to monitor heart rhythms and provide real-time data to healthcare providers, enabling timely interventions for cardiac conditions.
Yes, these devices are designed to be safe and effective when used as directed by a healthcare professional. They undergo rigorous testing to ensure patient safety.
If your device malfunctions, contact your healthcare provider immediately for assistance. Do not attempt to repair the device yourself.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1487-2022 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1487-2022 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
