Medtronic recalls certain implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) with model DTPA2D1G due to rare risk of reduced or no energy output during high voltage therapy, potentially affecting device effectiveness.
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 specific implantable cardioverter defibrillators (ICDs) and cardiac resynchronization therapy defibrillators (CRT-Ds) with model number DTPA2D1G. This recall is due to a rare risk that the device might not deliver enough energy during high voltage therapy, which could affect its ability to treat heart conditions.
The device uses a specific glassed feedthrough that may cause reduced or no energy output during high voltage therapy (typically 0-12J). This could lead to the device failing to treat heart conditions effectively, though this is a rare occurrence.
People with implantable cardioverter defibrillators (ICDs) or cardiac resynchronization therapy defibrillators (CRT-Ds) using the DTPA2D1G model. Those most at risk are patients who have recently had the device implanted or are currently using the device.
Check if your device has the model number DTPA2D1G. The lot and serial numbers listed are RTH602452S, RTH602446S, RTH602443S, RTH602454S, and RTH602442S. The device was sold with the GTIN 00763000501044.
Identify if your device has the model number DTPA2D1G.
This recall involves a rare risk of reduced or no energy output during high voltage therapy, which could affect device effectiveness. However, it is not a risk of serious injury in normal use.
Check if your device has the model number DTPA2D1G. The lot and serial numbers listed are RTH602452S, RTH602446S, RTH602443S, RTH602454S, and RTH602442S. The device was sold with the GTIN 00763000501044.
The recall does not specify a remedy, so you should contact Medtronic directly for guidance.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-1775-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1775-2023 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.
