Medtronic Neuromodulation: Medical Device Recall in 2024 - (Recall #: Z-1691-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator

Product Classification:

Class II

Date Initiated: March 28, 2024

Date Posted: May 8, 2024

Recall Number: Z-1691-2024

Event ID: 94338

Reason for Recall:

inability to reprogram one device

Status: Ongoing

Product Quantity: 1 unit

Code Information:

UDI/DI 00643169781719

Distribution Pattern:

International distribution in the country of UK.

Voluntary or Mandated:

Voluntary: Firm initiated