Medtronic Cardiac Rhythm and Heart Failure (CRHF) devices for medical use
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 Cardiac Rhythm and Heart Failure (CRHF) devices are medical devices used for cardiac rhythm management and heart failure treatment. These devices include pacemakers, defibrillators, and other cardiac monitoring systems.
These devices are medical devices designed for therapeutic use and are not dangerous to the general public. They are intended for specific medical conditions and require professional medical supervision.
Patients with cardiac rhythm disorders or heart failure conditions
Check for the Medtronic brand, model numbers (e.g., DDPA2D1), and serial numbers (e.g., RSL600237S) on the device or its packaging.
Identify the device model and serial number from the product label or packaging.
Verify the model number (e.g., DDPA2D1) and serial number (e.g., RSL600237S) against the official Medtronic product database.
Ensure the device is within the warranty period and has valid medical certification.
Medtronic CRHF devices are medical devices designed for cardiac rhythm management and heart failure treatment, including pacemakers, defibrillators, and cardiac monitoring systems.
Ensure the device has the correct model number and serial number, and that it is within the warranty period and has valid medical certification.
Contact your healthcare provider or Medtronic customer support immediately for assistance.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1485-2022 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1485-2022 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.
