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[Recalled] Bd Veritor Plus Analyzer — Increased risk or new adverse events | Health Canada 2022-01-17
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Bd Veritor Plus Analyzer |
|---|---|
| Category | Medical devices |
| Issuing authority | HC |
| Reference | 63828 |
| Country of notice | Canada |
| Risk level | Type II |
| Hazard type | recall |
| Notice date | 17 January 2022 |
Why it was recalled
According to the HC notice, the identified hazard is: Increased risk or new adverse events
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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