Health CanadaType II
Allura Xper FD10/10 - Main Unit, Allura Xper FD10, Allura Xper FD20 - Main Unit ...
Published: August 2, 2018Recall ID: 58183Category: generalCountry: Canada
Reason for Recall / Hazard
Medical devices
Product Description & Identification
Allura Xper FD10/10 - Main Unit, Allura Xper FD10, Allura Xper FD20 - Main Unit and Allura Xper FD20/10 System - Main Unit (2018-07-17)
Additional Source Details
| Field | Value |
|---|---|
| N I D | 58183 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd1010-main-unit-allura-xper-fd10-allura-xper-fd20-main-unit-and-allura |
| Issue | Medical devices |
| Title | Allura Xper FD10/10 - Main Unit, Allura Xper FD10, Allura Xper FD20 - Main Unit and Allura Xper FD20/10 System - Main Unit (2018-07-17) |
| Archived | 0 |
| Category | Medical devices |
| Last updated | 2018-08-02 |
| Organization | Medical devices |
| Recall class | Type II |