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[Recalled] LOGIQ P6 Ultrasound System - Main Unit and LOGIQ P6 Ultrasound System - Console Upgrade to BT09 (2018-12-27) — Medical devices | Health Canada 2019-01-23
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | LOGIQ P6 Ultrasound System - Main Unit and LOGIQ P6 Ultrasound System - Console Upgrade to BT09 (2018-12-27) |
|---|---|
| Category | Medical devices |
| Issuing authority | HC |
| Reference | 58610 |
| Country of notice | Canada |
| Risk level | Type II |
| Hazard type | recall |
| Notice date | 23 January 2019 |
Why it was recalled
According to the HC notice, the identified hazard is: Medical devices
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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