LiquiBandFIX8® recall in Canada: premature failure
In plain language
This recall involves the LiquiBandFIX8® Open Hernia Mesh Fixation Device sold in Canada. It's being recalled because of premature failure, where glue may leak from the device. Contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
LiquiBandFIX8® Open Hernia Mesh Fixation Device
Model: FX002
Lot: P00221182, P00221313, P00221396, P00221600, P00221756, P00221983, P00225605, P00225801, P00226740
Why this matters
Premature failure
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: P00221182, P00221313, P00221396, P00221600, P00221756, P00221983, P00225605, P00225801, P00226740
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: FX002
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?
Premature failure
What should consumers do?
Contact the manufacturer for 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. Premature failure
When was this product recalled?
This product was recalled on February 11, 2022.
Is the ADVANCED MEDICAL SOLUTIONS LIMITED brand affected by this recall?
Yes, ADVANCED MEDICAL SOLUTIONS LIMITED products are affected by this recall. This recall involves the LiquiBandFIX8® Open Hernia Mesh Fixation Device sold in Canada. It's being recalled because of premature failure, where glue may leak from the device. Contact the manufacturer for more information.