Medtronic recalls specific MRI-conditional defibrillators due to rare risk of device malfunction. Affected models include DTPB2QQ with serial numbers RTK602501S and RTK602506S.
Under rare circumstances, the component may be susceptible to a failure mechanism that could impact device performance, including potential loss of function.
Medtronic is recalling a specific type of implantable defibrillator that can rarely malfunction during MRI scans. This could lead to loss of device function, but the risk is very low and only affects a small number of units.
The device has a rare failure mechanism that could cause it to stop working properly during MRI scans. This might result in loss of function, but it's an uncommon occurrence and not a direct safety threat.
People with this specific implantable defibrillator model who have undergone MRI scans or are scheduled for one. Those with the model number DTPB2QQ and serial numbers RTK602501S or RTK602506S are most at risk.
Check if your defibrillator has the model number DTPB2QQ and serial numbers RTK602501S or RTK602506S. This specific model includes MRI SureScan technology and Bluetooth wireless telemetry.
Identify your defibrillator's model number and serial number to confirm if it matches DTPB2QQ with serial numbers RTK602501S or RTK602506S.
The recall states there is a rare risk of device malfunction during MRI scans, but it does not indicate a risk of serious injury or death. The hazard is described as low risk.
The recall does not specify any action steps for affected devices. You should check your device details to confirm if it is affected.
Your device is affected if it has the model number DTPB2QQ and serial numbers RTK602501S or RTK602506S.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0926-2021 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0926-2021 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.
