Medical Device Recall: Penumbra JET 7 Reperfusion Catheter and Penumbra Hi-Flow Aspiration Tubing

Press Release

By:

Ref: Health Canada

Published: 12/30/2020

Medical Device Recall: Penumbra JET 7 Reperfusion Catheter and Penumbra Hi-Flow Aspiration Tubing
 
Starting date: December 15, 2020
Posting date: December 30, 2020
Type of communication: Medical Device Recall
Subcategory: Medical Device
Hazard classification: Type I
Source of recall: Health Canada
Issue: Medical Devices
Audience: General Public, Healthcare Professionals, Hospitals
Identification number: RA-74671

Last updated:

2020-12-30
  1. Penumbra JET 7 Reperfusion Catheter
  2. Penumbra JET 7 Reperfusion Catheter and Penumbra Hi-Flow Aspiration Tubing

The Catheter may become susceptible to distal tip damage during use. Distal tip damage in conjunction with pressurization or contrast injection may result in potential vessel damage, and subsequent patient injury or death.

 
  • All lots.

5MAXJET7

Manufacturer
Penumbra Inc. 1351 Harbor Bay Parkway Alameda 94502 California UNITED STATES




 
 
 
  • All lots.

5MAXJET7KIT

Manufacturer
Penumbra Inc. 1351 Harbor Bay Parkway Alameda 94502 California UNITED STATES