Portex Acapella Dh (green) Vibratory Pep Device With Mouthpiece (2020-12-18)

The Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece is being recalled across Canada. The device is used to help clear airway secretions through vibration and positive expiratory pressure. The recall was issued due to issues classified as a Class I medical device concern, which indicates a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-01-07

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4df0fe30-7d60-4e4b-bbfc-15c24c13253d