PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: May 12, 2021 Initiated: March 25, 2021 #Z-1535-2021

Product Description

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.

Reason for Recall

There is a potential for unintended heating that can occur with the Intellis Model 97755 Recharger.

Details

Recalling Firm
Medtronic Neuromodulation
Units Affected
79,616 units
Distribution
Worldwide distribution.
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
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.. Recalled by Medtronic Neuromodulation. Units affected: 79,616 units.
Why was this product recalled?
There is a potential for unintended heating that can occur with the Intellis Model 97755 Recharger.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 12, 2021. Severity: Moderate. Recall number: Z-1535-2021.