Medtronic recalls Percept PC BrainSense Implantable Neurostimulator Model B35200 due to communication issues with clinical programmer systems. Affected devices may not function properly.
The Implantable Neurostimulator (INS) cannot communicate with the clinical programmer and/or the patient programmer system.
Medtronic is recalling Percept PC BrainSense Implantable Neurostimulators with model B35200. This device may not communicate with the patient's programming system, potentially causing treatment issues.
The device may not communicate with the clinical programmer or patient programmer system. This could lead to treatment issues if the device does not function properly.
Patients with Medtronic Percept PC BrainSense Implantable Neurostimulators model B35200 are affected. Those who have the device and use it for medical treatment are most at risk.
Check for model B35200 on the device. The serial number starts with NPI708734H and the expiration date is 10/28/2022.
Look for model B35200 on the device label.
The model number is B35200.
Check for model B35200 on the device label. The serial number starts with NPI708734H and the expiration date is 10/28/2022.
The recall does not specify a remedy, so contact Medtronic 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-1129-2022 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-1129-2022 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.
