Health Canada — Medical Devices · Canada · 2022-08-15 · Type II
🏛Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Reported risk: Connection issue for Vanta pain pc implantable neurostimulators when transplanted in the same patient. "Too many devices" error will appear from Clinician Programmer Application (CPA) when there is more than 1 Vanta ins detected by the clinician telemetry module. Current Vanta labeling does not include information with respect to what the "too many devices found" informational message means or how to troubleshoot it. Recall start date: August 4, 2022
Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.
ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.