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 |
601814RE |
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