Home/Recalls/CANADA-61978
Health CanadaType II

Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece (2020-12-18)

Published: January 7, 2021Recall ID: 61978Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece (2020-12-18)

Additional Source Details

FieldValue
N I D61978
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/portex-acapella-dh-green-vibratory-pep-device-mouthpiece-2020-12-18
IssueMedical devices
Title Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece (2020-12-18)
Archived0
CategoryMedical devices
Last updated2021-01-07
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert