Medtronic recalls Percepta CRT-P MRI SureScan devices with specific serial numbers due to potential reset from timing interaction between EffectivCRT Diagnostic and Ventricular Safety Pacing feature. Affected units include 120+ models with serial numbers starting with RNU600... or RNU601...
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 CRT-P MRI SureScan devices that may reset due to a timing interaction between the EffectivCRT Diagnostic and Ventricular Safety Pacing feature. This could cause the device to reset unexpectedly, potentially affecting heart rhythm management. The recall affects specific models with serial numbers listed in the notice.
The device may reset unexpectedly due to a timing interaction between the EffectivCRT Diagnostic and Ventricular Safety Pacing feature. This could cause the device to malfunction, potentially affecting heart rhythm management, but does not cause immediate injury or death.
Heart failure patients with implanted Percepta CRT-P MRI SureScan devices are most at risk. The recall affects specific models with serial numbers starting with RNU600 or RNU601.
Check if your device has a serial number starting with RNU600 or RNU601. The affected models include Percepta CRT-P MRI SureScan devices with specific serial numbers listed in the recall notice.
Look for the serial number on your device, which starts with RNU600 or RNU601.
If your device is affected, contact Medtronic directly for further instructions.
The device may reset unexpectedly due to a timing interaction between the EffectivCRT Diagnostic and Ventricular Safety Pacing feature, but it does not cause immediate injury or death.
Contact Medtronic directly for further instructions.
The recall includes 120+ specific models with serial numbers starting with RNU600 or RNU601.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2414-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2414-2018 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.
