Health product recall

ANGIOGUARD™ RX Emboli Capture Guidewire System

Brand(s)
Dernière mise à jour

Summary

Produit
ANGIOGUARD™ RX Emboli Capture Guidewire System
Problème
Medical devices - Performance issue
Ce qu’il faut faire

Contact the manufacturer if you require additional information.

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

ANGIOGUARD™ RX Emboli Capture Guidewire System

35264226
35264224

601814RE
501814RE

Problème

Cordis is recalling specific lots of ANGIOGUARD™ RX / XP Emboli Capture Guidewire System, Cordis has identified that there is a potential for separation of the ANGIOGUARD™ RX / XP delivery system and capture sheath. The potential impacts of separation include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke, while a replacement device is prepared.

Recall start date: March 15, 2023

Additional information

Details
Original published date: 2023-03-28
Type d’avis ou de rappel
Health product recall
Catégorie
Health product - Medical device - Cardiovascular
Entreprises

Cordis Us Corp.

14201 Nw 60th Ave., Miami Lakes, Florida, United States, 33014

Published by
Health Canada
Audience
Healthcare
Classe de rappel
Type I
Identification number
RA-73400