Health CanadaType II
Constellation® UltraVit® and HyperVit® Vitrectomy Probe
Published: September 26, 2025Recall ID: 78133Category: generalCountry: Canada
Reason for Recall / Hazard
Labelling and packaging - Performance
Product Description & Identification
Constellation® UltraVit® and HyperVit® Vitrectomy Probe
Affected Products
Constellation® UltraVit® and HyperVit® Vitrectomy Probe
Additional Source Details
| Field | Value |
|---|---|
| N I D | 78133 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/constellationr-ultravitr-and-hypervitr-vitrectomy-probe |
| Issue | Labelling and packaging - Performance |
| Title | Constellation® UltraVit® and HyperVit® Vitrectomy Probe |
| Product | Constellation® UltraVit® and HyperVit® Vitrectomy Probe |
| Archived | 0 |
| Category | Ophthalmology |
| Last updated | 2025-09-26 |
| Organization | Medical devices |
| Recall class | Type II |