Constellation® UltraVit® and HyperVit® Vitrectomy Probe
In plain language
This recall involves Constellation® UltraVit® and HyperVit® Vitrectomy Probes sold in Canada. They are being recalled because they may unexpectedly fail to cut during use. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer if you require additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Performance issue leading to potential for increased traction on vitreous and/or retina that could lead to holes/tears.
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Performance issue leading to potential for increased traction on vitreous and/or retina that could lead to holes/tears.
What should consumers do?
Stop using the product immediately. Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Performance issue leading to potential for increased traction on vitreous and/or retina that could lead to holes/tears.
When was this product recalled?
This product was recalled on September 26, 2025.
Is the Alcon Laboratories Inc. brand affected by this recall?
Yes, Alcon Laboratories Inc. products are affected by this recall. This recall involves Constellation® UltraVit® and HyperVit® Vitrectomy Probes sold in Canada. They are being recalled because they may unexpectedly fail to cut during use. Stop using the product and contact the manufacturer for more information.