Quadrox-i/-id Oxygenators

Quadrox-I/-Id Oxygenators Recall Quadrox-I/-Id Oxygenators are being recalled across Canada due to sterility concerns that could affect their performance. These medical devices are used during certain medical procedures where oxygenation is needed. The recall is classified as Class I, indicating a serious potential health risk.

Product

Quadrox-I/-Id Oxygenators

Reason

Performance - Sterility

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2023-04-06

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6eb7c571-e596-49eb-a443-0fdac3ce6dd2