Health CanadaType II
Fred® Flow Re-Direction Endoluminal Device
Published: November 4, 2024Recall ID: 74058Category: generalCountry: Canada
Reason for Recall / Hazard
Performance
Product Description & Identification
Fred® Flow Re-Direction Endoluminal Device
Additional Source Details
| Field | Value |
|---|---|
| N I D | 74058 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/fredr-flow-direction-endoluminal-device |
| Issue | Performance |
| Title | Fred® Flow Re-Direction Endoluminal Device |
| Product | Fred® Flow Re-Direction Endoluminal Device |
| Archived | 0 |
| Category | Neurology |
| Last updated | 2024-11-04 |
| Organization | Medical devices |
| Recall class | Type II |