Medtronic recalls certain implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) with model DTMA1Q1. These devices have a rare potential for reduced or no energy output during high voltage therapy, which could affect treatment effectiveness. The recall includes specific lot and serial numbers listed in the notice.
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 DTMA1Q1. These devices have a rare risk of reduced or no energy output during high voltage therapy, which could impact treatment effectiveness. If you own one of these devices, you should contact Medtronic for further instructions.
The devices have a specific (glassed) feedthrough that can cause reduced or no energy output during high voltage therapy (typically 0-12J). This could affect the device's ability to deliver effective shocks when needed, potentially impacting treatment effectiveness for heart conditions.
Individuals who own or use Medtronic ICDs or CRT-Ds with model number DTMA1Q1 and specific lot/serial numbers listed in the recall notice. The risk is rare and not expected to cause serious injury.
Check if your device has the model number DTMA1Q1. The recall includes specific lot and serial numbers listed in the notice (e.g., RPS205974H, RPS208665H, etc.).
Verify your device's model number is DTMA1Q1. The recall includes specific lot and serial numbers listed in the notice.
Reach out to Medtronic for instructions on next steps, as the recall includes specific lot and serial numbers.
The model number is DTMA1Q1.
Check if your device has model number DTMA1Q1 and verify your lot/serial number against the list provided in the recall notice.
If your device is not listed in the recall notice, it is not affected by this recall.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1755-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1755-2023 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.
