Home/Recalls/CANADA-58788
Health CanadaType III

Compress Device Centering Sleeve, Compress Device and Compress Device Short Anti...

Published: January 9, 2019Recall ID: 58788Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Compress Device Centering Sleeve, Compress Device and Compress Device Short Anti-Rotation Spindle, Anti-Rotation Elliptical Spindle, and Compress Instrument Drill for Anti-Rotation Pin (2018-12-13)

Additional Source Details

FieldValue
N I D58788
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/compress-device-centering-sleeve-compress-device-and-compress-device-short-anti
IssueMedical devices
Title Compress Device Centering Sleeve, Compress Device and Compress Device Short Anti-Rotation Spindle, Anti-Rotation Elliptical Spindle, and Compress Instrument Drill for Anti-Rotation Pin (2018-12-13)
Archived0
CategoryMedical devices
Last updated2019-01-09
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert