Medtronic recalls certain implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) with model DTMA2D1. A rare potential for reduced or no energy output during high voltage therapy may cause treatment failure. Affected units have 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 DTMA2D1. These devices have a rare potential for reduced or no energy output during high voltage therapy, which could lead to treatment failure. The recall affects specific units with listed serial numbers.
The hazard involves a rare potential for reduced or no energy output during high voltage therapy (typically 0-12J) in these devices. This could lead to treatment failure if the device is unable to deliver the necessary energy to the heart during critical events.
People with Medtronic implantable cardioverter defibrillators (ICDs) or cardiac resynchronization therapy defibrillators (CRT-Ds) manufactured with a specific glassed feedthrough. The recall covers specific units identified by serial numbers listed in the recall.
Check if your device has the model number DTMA2D1. The recall includes specific units with serial numbers listed in the recall notice. The GTIN is 00643169837621.
Identify your device model by checking the label on the device or its packaging. The affected devices have model number DTMA2D1.
Compare your device's serial number with the list of affected serial numbers provided in the recall notice.
The affected devices have model number DTMA2D1.
Check your device's model number and compare it with DTMA2D1. Then verify your serial number against the list of affected serial numbers provided in the recall notice.
Contact Medtronic directly to confirm if your device is affected and follow their 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-1757-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1757-2023 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.
