Penumbra Jet 7 Reperfusion Catheter And Penumbra Hi-flow Aspiration Tubing (2020-12-15)

Recall Summary Penumbra has recalled the JET 7 Reperfusion Catheter and Hi-Flow Aspiration Tubing across Canada due to a medical device issue. These products are used in medical procedures to treat stroke patients by removing blood clots from arteries. The recall affects all units of these devices distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-12-30

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f190e6cb-219b-4b3e-b928-e49d40df9580