Constellation® Ultravit® And Hypervit® Vitrectomy Probe
Recall Summary Constellation® UltraVit® and HyperVit® Vitrectomy Probes are being recalled across Canada due to labeling and packaging issues that affect product performance. These devices are used during eye surgery to remove vitreous material from the eye. The recall is classified as Class I, the most serious category.
- Product
- Constellation® UltraVit® and HyperVit® Vitrectomy Probe
- Reason
- Labelling and packaging - Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-09-26
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1ede8c16-cc36-470a-9171-30b2725da78c