Medtronic recalls specific implantable defibrillators (model DTPA2Q1) due to potential weld cracks causing manufacturing failures. Affected units have unique serial numbers and GTINs. Contact Medtronic for details.
Potential for manufacturing defect. Weld crack led to devices failing at the leak check step in manufacturing.
Medtronic is recalling certain implantable cardioverter defibrillators (model DTPA2Q1) because a manufacturing defect may cause weld cracks that fail during quality checks. This could lead to device malfunction, though the risk is not immediate.
A manufacturing defect may cause weld cracks in the device. These cracks can lead to failure during the leak check step in production, potentially causing the device to malfunction.
People with the specific model DTPA2Q1 implantable cardioverter defibrillators (serial numbers listed) are affected. Those who have had the device implanted are most at risk.
Check for the model number DTPA2Q1 on the device label. Look for the specific serial numbers listed: RTD607545S, RTD607549S, RTD607551S, RTD607363S, RTD607364S, RTD607367S, RTD607369S, RTD607370S, RTD607374S, RTD607404S, RTD607405S.
Look for the model number DTPA2Q1 and the specific serial numbers listed in the recall notice.
The recall does not require immediate stopping of use. However, affected units should be checked with Medtronic for further instructions.
Contact Medtronic directly using the provided information to determine if your device is affected and what steps to take.
Check the model number DTPA2Q1 and the specific serial numbers listed in the recall notice.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2193-2024 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2193-2024 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.
