Prevalon Airtap Booster Pump

Prevalon Airtap Booster Pump Recall Prevalon Airtap Booster Pump devices are being recalled in Canada because they may fail to deliver the correct pressure needed to inflate air mattresses properly. This defect could result in mattresses not functioning as intended for pressure relief or patient positioning. The recall affects all Prevalon Airtap Booster Pump units distributed across Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-09-05

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d82aa760-8477-45a5-a7c1-ee4785c05fdb