Medtronic Neuromodulation Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargeable neurostimulators: Intellis with AdaptiveStim Technology Model 97715 Implanted Neurostimulator Intellis Model 97716 Implanted Neurostimulator. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargeable neurostimulators: Intellis with AdaptiveStim Technology Model 97715 Implanted Neurostimulator Intellis Model 97716 Implanted Neurostimulator.
Brand
Medtronic Neuromodulation
Lot Codes / Batch Numbers
All serial numbers
Products Sold
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Medtronic Neuromodulation is recalling Intellis Model 97755 Recharger - Product Usage: designed to charge the following Medtronic rechargea due to There is a potential for unintended heating that can occur with the Intellis Model 97755 Recharger.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There is a potential for unintended heating that can occur with the Intellis Model 97755 Recharger.
Recommended Action
Per FDA guidance
Beginning 25-Mar-2021, Medtronic began notifying physicians in the US and consignees OUS via mail, email, fax, and/or personal visit by Medtronic personnel. In the US, each implanting physician was sent the medical device correction letter, the patient quick guide, and the customer confirmation form. Outside the US, the medical device correction letter, the patient quick guide, and the customer confirmation form were sent to the healthcare facilities. Additionally, on an ongoing basis, the patient quick guide will be provided with each replacement recharger.
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