Home/Recalls/CANADA-73893
Health CanadaType II

Simplexa Direct Amplification Disc Kit

Published: July 4, 2023Recall ID: 73893Category: generalCountry: Canada

Reason for Recall / Hazard

Performance

Product Description & Identification

Simplexa Direct Amplification Disc Kit

Additional Source Details

FieldValue
N I D73893
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/simplexa-direct-amplification-disc-kit-0
IssuePerformance
TitleSimplexa Direct Amplification Disc Kit
ProductSimplexa Direct Amplification Disc Kit
Archived1
CategoryMicrobiology
Last updated2023-07-04
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert