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[Recalled] Labsscreen Multi — Medical devices | Health Canada 2017-05-16

recall health-canada medical-devices canada

This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.

Recall details

ProductLabsscreen Multi
CategoryMedical devices
Issuing authorityHealth Canada
Reference44471
Country of noticeCanada
Risk levelType III
Hazard typerecall
Notice date16 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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