Health CanadaType II
IntraClude Intra-Aortic Occlusion Device (2019-01-21)
Published: March 8, 2019Recall ID: 59061Category: generalCountry: Canada
Reason for Recall / Hazard
Medical devices
Product Description & Identification
IntraClude Intra-Aortic Occlusion Device (2019-01-21)
Additional Source Details
| Field | Value |
|---|---|
| N I D | 59061 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/intraclude-intra-aortic-occlusion-device-2019-01-21 |
| Issue | Medical devices |
| Title | IntraClude Intra-Aortic Occlusion Device (2019-01-21) |
| Archived | 0 |
| Category | Medical devices |
| Last updated | 2019-03-08 |
| Organization | Medical devices |
| Recall class | Type II |