Medtronic Recharger Kits (Medtronic) – Charging Session Issue (2024)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulators. The Rechargers are used with Neurostimulator Inceptiv INS Model 977119 and Percept RC INS Model B35300 as part of the Deep Brain Stimulation (DBS) system. WR9220A is used with InterStim Micro, Model 97810, as part of Pelvic Health system
Brand
Medtronic Neuromodulation
Lot Codes / Batch Numbers
RS6230 - GTIN 00763000564353, Serial numbers: NRA010637N, NRA011389N, NRA013260N, NRA013664N, NRA013924N, NRA014318N, NRA014347N, NRA015823N, NRA015861N, NRA015864N, NRA016334N, NRA016413N, NRA016430N, NRA016432N, NRA016778N, RA017002N, NRA017048N, NRA017227N, NRA017232N, NRA017685N, NRA018697N, NRA018731N, NRA018906N, NRA018936N, NRA018992N, NRA019019N, NRA019026N, NRA019963N, NRA019967N, NRA019968N, NRA019970N, NRA019983N, NRA010657N, NRA012367N, NRA012898N, NRA012915N, NRA013490N, NRA013643N, NRA013877N, NRA013878N, NRA013880N, NRA014248N, NRA014741N, NRA015127N, NRA015142N, NRA010659N, NRA010661N, NRA010663N NRA016424N, NRA016425N, NRA016426N, NRA016431N, RA016433N, NRA021324N. RS7230 - GTIN 00763000540289, Serial numbers: NRA010640N, NRA010650N, NRA010656N: NRA011591N, NRA012896N, NRA012910N, NRA012925N, NRA013884N, NRA010633N, NRA010635N, NRA010641N, NRA010642N, NRA010646N, NRA010652N, NRA010653N, NRA010654N, NRA010655N, NRA010658N, NRA010660N, NRA010664N, NRA010666N, NRA010667N, NRA010668N, NRA010669N, NRA010881N, NRA011216N, NRA011293N, NRA011393N, NRA011713N, NRA011853N, NRA012184N, NRA012897N, NRA012909N, NRA012911N, NRA012912N, NRA012913N, NRA012914N, NRA013502N, NRA013602N, NRA013603N, NRA013634N, NRA013635N, NRA013638N, NRA013639N, NRA013879N, NRA013883N, NRA013899N, NRA013952N, NRA014259N, NRA014944N, NRA015858N, NRA015904N, NRA011189N, NRA011238N, NRA012130N, NRA012185N, NRA012366N, NRA013543N, NRA014132N, NRA014222N, GTIN 0763000827533, Serial numbers: NRA010558N, NRA010627N, NRA015360N, NRA013633N.
Products Sold
RS6230 - GTIN 00763000564353, Serial numbers: NRA010637N; NRA011389N; NRA013260N; NRA013664N; NRA013924N; NRA014318N; NRA014347N; NRA015823N; NRA015861N; NRA015864N; NRA016334N; NRA016413N; NRA016430N; NRA016432N; NRA016778N; RA017002N; NRA017048N; NRA017227N; NRA017232N; NRA017685N; NRA018697N; NRA018731N; NRA018906N; NRA018936N; NRA018992N; NRA019019N; NRA019026N; NRA019963N; NRA019967N; NRA019968N; NRA019970N; NRA019983N; NRA010657N; NRA012367N; NRA012898N; NRA012915N; NRA013490N; NRA013643N; NRA013877N; NRA013878N; NRA013880N; NRA014248N; NRA014741N; NRA015127N; NRA015142N, NRA010659N; NRA010661N; NRA010663N NRA016424N; NRA016425N; NRA016426N; NRA016431N; RA016433N; NRA021324N. RS7230 - GTIN 00763000540289, Serial numbers: NRA010640N; NRA010650N; NRA010656N: NRA011591N; NRA012896N; NRA012910N; NRA012925N; NRA013884N; NRA010633N; NRA010635N; NRA010641N; NRA010642N; NRA010646N; NRA010652N; NRA010653N; NRA010654N; NRA010655N; NRA010658N; NRA010660N; NRA010664N; NRA010666N; NRA010667N; NRA010668N; NRA010669N; NRA010881N; NRA011216N; NRA011293N; NRA011393N; NRA011713N; NRA011853N; NRA012184N; NRA012897N; NRA012909N; NRA012911N; NRA012912N; NRA012913N; NRA012914N; NRA013502N; NRA013602N; NRA013603N; NRA013634N; NRA013635N; NRA013638N; NRA013639N; NRA013879N; NRA013883N; NRA013899N; NRA013952N; NRA014259N; NRA014944N; NRA015858N; NRA015904N; NRA011189N; NRA011238N; NRA012130N; NRA012185N; NRA012366N; NRA013543N; NRA014132N; NRA014222N; GTIN 0763000827533, Serial numbers: NRA010558N; NRA010627N; NRA015360N; NRA013633N.
Medtronic Neuromodulation is recalling Medtronic Recharger Kits, RS6230, RS7230, and RS5220A, containing components WR9230 and WR9220A Rec due to The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.
Recommended Action
Per FDA guidance
The recalling firm issued letters dated September 2024 on 9/18/2024 via UPS 2-Day Air. The letter explained the issue, product scope, and the customer actions. The actions included: (1) Identify and quarantine all unused affected WR Kits. Attachment A of the letter provides guidance on identifying potentially affected devices; (2) Return all unused affected WR Kits using the instructions in the enclosed customer confirmation form and contact Medtronic Customer Service to obtain a replacement WR Kit; (3) Direct patients who cannot establish a recharge session using their WR to promptly contact Medtronic Customer Service to obtain a replacement WR Kit; (4) Complete the enclosed Customer Confirmation Form; (5) Share this notice with all those who need to be aware of this issue within or outside your organization or to any organization where the potentially affected product has been transferred or distributed and maintain a copy of this notice in your records. Medtronic initiated communication of the potential issue via physical mailing to one (1) customer beginning on 08-July-2025 in the U.S.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026