International safety notice

Medtronic Percept RC and Medtronic Inceptiv wireless recharger (hereinafter referred to as “Recharge”) Rechargers and other products with serial numbers that underwent specific rework during manufacture When using the neurostimulator, there may be a problem where communication with the neurostimulator and charging session cannot be established. vinegar. We will voluntarily recall unused products with specific serial numbers that may be affected by this problem. Please note that the recharger currently in use is not affected by this problem and operates normally, so it is not subject to this voluntary recall. vinegar.

Japan / PMDA Recalls · JPN · Sep 19, 2024

Key facts

Title Medtronic Percept RC and Medtronic Inceptiv wireless recharger (hereinafter referred to as “Recharge”) Rechargers and other products with serial numbers that underwent specific rework during manufacture When using the neurostimulator, there may be a problem where communication with the neurostimulator and charging session cannot be established. vinegar. We will voluntarily recall unused products with specific serial numbers that may be affected by this problem. Please note that the recharger currently in use is not affected by this problem and operates normally, so it is not subject to this voluntary recall. vinegar.
Regulator Japan / PMDA Recalls
Country JPN
Brand Common names: (1) Electrical brain stimulator for tremors, (2) Implantable pain relief stimulator Brand name: (1) Medtronic Percept RC (2) Medtronic Inceptiv
Manufacturer Japan Medtronic Co., Ltd.
Models NRA016431N, NRA010659N, NRA013543N, NRA012130N, NRA011189N, RS6230, NRA014222N, NRA012366N, NRA010661N, NRA011238N, NRA016424N, NRA016433N and 6 more
Date Sep 19, 2024
Regulator page info.pmda.go.jp

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices