Product Wiki · Recalls · Health Canada — Medical Devices

Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece… — recall 61978

Health Canada — Medical Devices · Canada · 2021-01-07 · Type II

As described by Health Canada — Medical Devices: Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece (2020-12-18)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
61978
Date of alert
2021-01-07
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Smiths Medical received 1 complaint alleging that one lot of Portex Acapella DH (green) Vibratory PEP Device with Mouthpiece (model number 21-1530) shipping boxes incorrectly contained Portex Acapella DM (blue) Vibratory Pep Device with Mouthpiece devices (model number 21-1015).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/portex-acapella-dh-green-vibra

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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