Health CanadaType II
Kodak Directview DR 7500 Dual Detector System (using version 5 software) (2014-0...
Published: March 21, 2014Recall ID: 51385Category: generalCountry: Canada
Reason for Recall / Hazard
Medical devices
Product Description & Identification
Kodak Directview DR 7500 Dual Detector System (using version 5 software) (2014-02-21)
Additional Source Details
| Field | Value |
|---|---|
| N I D | 51385 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/kodak-directview-dr-7500-dual-detector-system-using-version-5-software-2014-02-21 |
| Issue | Medical devices |
| Title | Kodak Directview DR 7500 Dual Detector System (using version 5 software) (2014-02-21) |
| Archived | 1 |
| Category | Medical devices |
| Last updated | 2014-03-21 |
| Organization | Medical devices |
| Recall class | Type II |