Medtronic recalls Recharger Kits RS6230, RS7230, and RS5220A that may fail to enter recharging session upon first use. Affected units include specific serial numbers and models for deep brain stimulation and pelvic health systems.
The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.
Medtronic is recalling Recharger Kits (RS6230, RS7230, RS5220A) that may not charge properly when first used. This could prevent the device from working correctly for medical implants like deep brain stimulation systems.
The wireless rechargers in these kits may not enter a recharging session during the first use. This could prevent the device from charging properly, which might affect the medical implant's function over time.
Patients with deep brain stimulation (DBS) implants or pelvic health systems using the recalled recharger kits. Those with specific serial numbers listed in the recall are most at risk.
Check if your Medtronic Recharger Kit has the model numbers RS6230, RS7230, or RS5220A. Look for the specific serial numbers listed in the recall notice for deep brain stimulation or pelvic health systems.
Identify if your kit is RS6230, RS7230, or RS5220A by checking the product label.
Confirm if your kit's serial number matches the list provided in the recall notice for deep brain stimulation or pelvic health systems.
The wireless rechargers in these kits may not enter a recharging session upon first use, which could prevent proper charging of medical implants.
RS6230, RS7230, and RS5220A recharger kits used with specific medical implants like deep brain stimulation (DBS) systems or pelvic health systems.
Check the product label for the model number and compare the serial number against the list provided in the recall notice.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0372-2025 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0372-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
