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

Starting date:

December 18, 2020

Posting date:

January 7, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-74699

Last updated:
2021-01-07

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  Reason
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  Affected products

Affected Products 

Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece

Reason

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).

Affected products