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[Recalled] COBAS EGFR MUTATION TEST V2 — Inaccurate test or measurement results | Health Canada 2021-11-26
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | COBAS EGFR MUTATION TEST V2 |
|---|---|
| Category | Medical devices |
| Issuing authority | HC |
| Reference | 63663 |
| Country of notice | Canada |
| Risk level | Type II |
| Hazard type | recall |
| Notice date | 26 November 2021 |
Why it was recalled
According to the HC notice, the identified hazard is: Inaccurate test or measurement results
This Type II recall concerns Medical devices 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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