Product Wiki · Recalls · Health Canada — Medical Devices

GenoType MTBDR plus (2014-09-04) — recall 52348

Health Canada — Medical Devices · Canada · 2014-09-25 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
52348
Date of alert
2014-09-25
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Sale and advertisement of the unlicensed medical device GenoType MTBDR plus version 2.0 kit from Hain Lifescience GmbH.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/genotype-mtbdr-plus-2014-09-04

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.