ProductGuru Recalls

Official recall record

Inceptiv

Health Canada — Medical Devices · 2025-06-10 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-06-10
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Performing a switch device operation from the 97725 or 9772501 WENS using the A71300 SCS trialing app to transfer data (e.g. patient and lead information) to a new implanted Inceptiv or Intellis Pro Implantable Neurostimulator (INS) results in the A71400 CP app crashing and the INS becoming unusable when the transfer involves a predefined legacy lead option selected in the app that uses the forward slash character "/". Recall start date: May 28, 2025

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.