Health CanadaType II
Alcon Vitrectomy Products
Published: August 20, 2025Recall ID: 77941Category: generalCountry: Canada
Safety AlertHealth CanadaCanada
CanadaAlcon Vitrectomy Products
Recalling Firm: Medical devices
Reason for Recall / Hazard
Sterility
Product Description & Identification
Alcon Vitrectomy Products
Additional Source Details
| Field | Value |
|---|---|
| N I D | 77941 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/alcon-vitrectomy-products |
| Issue | Sterility |
| Title | Alcon Vitrectomy Products |
| Product | Alcon Vitrectomy Products |
| Archived | 0 |
| Category | Ophthalmology |
| Last updated | 2025-08-20 |
| 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 - Alcon Vitrectomy Products Check if your household is affected: https://therecallfile.com/recalls/alcon-vitrectomy-products/CANADA-77941
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