Teleflex Green Non-latex Robertazzi Nasopharyngeal Airway

Recall Summary Teleflex is recalling Green Non-Latex Robertazzi Nasopharyngeal Airway devices distributed across Canada due to a medical device issue. The recall is classified as Class I, indicating a serious safety concern. This product is used in medical settings to help maintain airway passages.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-02-01

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5d9fcb51-4d99-4ec7-b42d-d75dbdb709f5