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[Recalled] Activa Clinician Programmer Application For Deep Brain Stimulation — Device compatibility | Health Canada 2022-08-02
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | Activa Clinician Programmer Application For Deep Brain Stimulation |
|---|---|
| Category | General hospital and personal use |
| Issuing authority | HC |
| Reference | 64430 |
| Country of notice | Canada |
| Risk level | Type II |
| Hazard type | recall |
| Notice date | 02 August 2022 |
Why it was recalled
According to the HC notice, the identified hazard is: Device compatibility
This Type II recall concerns General hospital and personal use products distributed in Canada and was recorded by HC. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Review the official notice to confirm whether your unit is affected.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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