Health CanadaType II
ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)
Published: November 25, 2021Recall ID: 63647Category: generalCountry: Canada
Safety AlertHealth CanadaCanada
CanadaALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)
Recalling Firm: Medical devices
Reason for Recall / Hazard
Software defect
Product Description & Identification
ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)
Additional Source Details
| Field | Value |
|---|---|
| N I D | 63647 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd10-and-fd2010-product-alluraclarity-family |
| Issue | Software defect |
| Title | ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY) |
| Product | ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY) |
| Archived | 0 |
| Category | Radiology |
| Last updated | 2021-11-25 |
| 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 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY) Check if your household is affected: https://therecallfile.com/recalls/allura-xper-fd10-and-fd20-10-product-of-alluraclarity-family/CANADA-63647
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