[Recalled] Precision Pointer Electromagnetic (EM)
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Precision Pointer Electromagnetic (EM) |
|---|---|
| Category | Neurology |
| Issuing authority | Health Canada — Medical Devices |
| Reference | 82702 |
| Country of notice | Canada |
| Authority classification | Type II |
| Notice date | 02 October 2026 |
Why it was recalled
According to the Health Canada — Medical Devices notice, the identified hazard is: Stryker has identified that the tip of the Precision Pointer EM may potentially fracture at the laser welding seam. To date, Stryker has received 60 complaints related to this issue.
This recall concerns Neurology products distributed in Canada and was recorded by Health Canada — Medical Devices. 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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