Health CanadaType III
IVOCLAR VIVADENT AG products (2016-07-01)
Published: July 19, 2016Recall ID: 55300Category: generalCountry: Canada
Safety AlertHealth CanadaCanada
CanadaIVOCLAR VIVADENT AG products (2016-07-01)
Recalling Firm: Medical devices
Reason for Recall / Hazard
Medical devices
Product Description & Identification
IVOCLAR VIVADENT AG products (2016-07-01)
Additional Source Details
| Field | Value |
|---|---|
| N I D | 55300 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/ivoclar-vivadent-ag-products-2016-07-01 |
| Issue | Medical devices |
| Title | IVOCLAR VIVADENT AG products (2016-07-01) |
| Archived | 1 |
| Category | Medical devices |
| Last updated | 2016-07-19 |
| Organization | Medical devices |
| Recall class | Type III |
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Overview
- Recalling FirmMedical devices
- Risk LevelType III
Recall Hazard Severity
Official Agency AlertCaution (Class III)
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🚨 SAFETY ALERT: Medical devices - IVOCLAR VIVADENT AG products (2016-07-01) Check if your household is affected: https://therecallfile.com/recalls/ivoclar-vivadent-ag-products-2016-07-01/CANADA-55300
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