Health CanadaType III
LiquiBandFIX8® Open Hernia Mesh Fixation Device
Published: February 11, 2022Recall ID: 63914Category: generalCountry: Canada
Reason for Recall / Hazard
Premature failure
Product Description & Identification
LiquiBandFIX8® Open Hernia Mesh Fixation Device
Additional Source Details
| Field | Value |
|---|---|
| N I D | 63914 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/liquibandfix8r-open-hernia-mesh-fixation-device |
| Issue | Premature failure |
| Title | LiquiBandFIX8® Open Hernia Mesh Fixation Device |
| Product | LiquiBandFIX8® Open Hernia Mesh Fixation Device |
| Archived | 0 |
| Category | General and plastic surgery |
| Last updated | 2022-02-11 |
| Organization | Medical devices |
| Recall class | Type III |