Health CanadaType II
Allura Xper Fd10 & Fd20 products
Published: December 13, 2021Recall ID: 63712Category: generalCountry: Canada
Safety AlertHealth Canada
Canada
Allura Xper Fd10 & Fd20 products
Recalling Firm: Medical devices
Reason for Recall / Hazard
Mechanical defect
Product Description & Identification
Allura Xper Fd10 & Fd20 products
Additional Source Details
| Field | Value |
|---|---|
| N I D | 63712 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-fd20-products |
| Issue | Mechanical defect |
| Title | Allura Xper Fd10 & Fd20 products |
| Product | Allura Xper Fd10 & Fd20 products |
| Archived | 0 |
| Category | Radiology |
| Last updated | 2021-12-13 |
| Organization | Medical devices |
| Recall class | Type II |
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Overview
- Recalling FirmMedical devices
- Risk LevelType II
Recall Hazard Severity
Official Agency AlertCaution (Class III)
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🚨 SAFETY ALERT: Medical devices - Allura Xper Fd10 & Fd20 products Check if your household is affected: https://therecallfile.com/recalls/allura-xper-fd10-fd20-products/CANADA-63712
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