HEALON GV PRO recall in Canada: Ocular injury risk
In plain language
This recall involves HEALON GV PRO (OVD) medical devices sold in Canada. It's being recalled because it may be difficult to remove from the eye, potentially causing increased post-operative intra-ocular pressure or ocular injury. There are also reports of potential clogging of phacoemulsification equipment tubing. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check lot numbers UE31408, UE31439, UE31559.
- Follow instructions from your healthcare professional or the manufacturer.
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Affected products
HEALON GV PRO (OVD)
Lot: UE31408, UE31439, UE31559
Why this matters
Ocular injury risk
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: UE31408, UE31439, UE31559
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Ocular injury risk
What should consumers do?
Stop using the product immediately. Check lot numbers UE31408, UE31439, UE31559. Follow instructions from your healthcare professional or the manufacturer.
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. Ocular injury risk
When was this product recalled?
This product was recalled on January 6, 2020.
Is the HEALON GV PRO brand affected by this recall?
Yes, HEALON GV PRO products are affected by this recall. This recall involves HEALON GV PRO (OVD) medical devices sold in Canada. It's being recalled because it may be difficult to remove from the eye, potentially causing increased post-operative intra-ocular pressure or ocular injury. There are also reports of potential clogging of phacoemulsification equipment tubing. Stop using the product and follow the return/repair steps in the official notice.