[Recalled] Labsscreen Multi — Medical devices | Health Canada 2017-05-16
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | Labsscreen Multi |
|---|---|
| Category | Medical devices |
| Issuing authority | Health Canada |
| Reference | 44471 |
| Country of notice | Canada |
| Risk level | Type III |
| Hazard type | recall |
| Notice date | 16 May 2017 |
Why it was recalled
According to the Health Canada notice, the identified hazard is: The LabScreen multi instruction for use (LM-MUTR-PI REV 8, released April 20, 2016) incorrectly states the capability to use the LabScan 3D instrument in conjunction with the LabScreen multi product.
This Type III recall concerns Medical devices products distributed in Canada and was recorded by Health Canada. 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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