Medtronic recalls Percepta Quad CRT-P MRI SureScan devices with specific serial numbers due to potential device reset from timing interactions between EffectivCRT Diagnostic and Ventricular Safety Pacing features. Affected units include 100+ models with serial numbers starting with RNP202329H.
Potential for a device reset to occur in Percepta CRT-P MRI SureScan and Percepta Quad CRT-P MRI SureScan due to a timing interaction between the EffectivCRT Diagnostic and the Ventricular Safety Pacing feature (VSP).
Medtronic is recalling Percepta Quad CRT-P MRI SureScan devices that may reset due to a timing interaction between the EffectivCRT Diagnostic and Ventricular Safety Pacing features. This could cause unintended device behavior but does not pose an immediate risk to patients.
The device may reset due to a timing interaction between the EffectivCRT Diagnostic and Ventricular Safety Pacing features. This could lead to unintended device behavior but does not cause injury or death in normal use.
Patients with implanted Percepta Quad CRT-P MRI SureScan devices who have specific serial numbers listed in the recall. The risk is low as the issue does not cause immediate harm.
Check if your device has a serial number starting with RNP202329H or similar patterns listed in the recall. The Percepta Quad CRT-P MRI SureScan devices are implantable pulse generators for heart failure patients.
Look for the serial number on your device, which starts with RNP202329H or similar patterns listed in the recall.
If your device is affected, contact Medtronic directly for further instructions.
No, this recall is low risk. The device may reset due to a timing interaction but does not cause injury or death in normal use.
Check if your device has a serial number starting with RNP202329H or similar patterns listed in the recall.
Contact Medtronic directly for further instructions. The recall does not require immediate action but should be addressed.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2413-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2413-2018 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.
