Medtronic recalls certain implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) with model DTMA2D4 that may have reduced energy output during high voltage therapy, potentially causing ineffective treatment. Affected units include specific serial numbers listed in the recall.
There is a rare potential for reduced- or no-energy output during high voltage (HV) therapy (typically 0-12J) in implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific (glassed) feedthrough, including currently available ICDs and CRT-Ds.
Medtronic is recalling certain implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) with model number DTMA2D4. These devices may have reduced energy output during high voltage therapy, which could lead to ineffective treatment. This is a rare but potential issue that requires attention.
The device may have a glassed feedthrough that causes reduced or no energy output during high voltage therapy (0-12J). This could result in ineffective treatment of heart rhythm issues, but the risk is rare and not life-threatening.
Patients with Medtronic ICDs or CRT-Ds manufactured with the DTMA2D4 model number are affected. The risk is rare and typically does not cause serious injury.
Check if your device has the model number DTMA2D4. The recall includes specific serial numbers listed in the official notice. If you have an implantable defibrillator, contact Medtronic for verification.
Verify your device model number is DTMA2D4. This recall includes specific serial numbers listed in the official notice.
Reach out to Medtronic directly to confirm if your device is affected and to receive instructions for next steps.
This recall involves a rare potential for reduced energy output during high voltage therapy, which could lead to ineffective treatment. However, it is not a risk of serious injury or death.
Check if your device has the model number DTMA2D4. The recall includes specific serial numbers listed in the official notice. Contact Medtronic for verification.
Contact Medtronic directly to confirm if your device is affected and to receive instructions for next steps.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1758-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1758-2023 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.
