Biodesign® Hiatal Hernia Graft recall in Canada: labelling error
In plain language
This recall involves Biodesign® Hiatal Hernia Grafts sold in Canada. It's being recalled because of a discrepancy between the product's actual shelf life and the shelf life printed on the label. This could lead to the product being used past its expiration date. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact the manufacturer, Cook Biotech Inc., for more information.
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Affected products
Biodesign® Hiatal Hernia Graft
Model: C-PHR-7X10-U
Lot: LB1579758
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: LB1579758
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: C-PHR-7X10-U
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?
This recall involves Biodesign® Hiatal Hernia Grafts sold in Canada. It's being recalled because of a discrepancy between the product's actual shelf life and the shelf life printed on the label. This could lead to the product being used past its expiration date. Stop using the product and follow the return/repair steps in the official notice.
What should consumers do?
Stop using the product immediately. Contact the manufacturer, Cook Biotech Inc., for more 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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on December 19, 2024.
Is the Cook Biotech Inc. brand affected by this recall?
Yes, Cook Biotech Inc. products are affected by this recall. This recall involves Biodesign® Hiatal Hernia Grafts sold in Canada. It's being recalled because of a discrepancy between the product's actual shelf life and the shelf life printed on the label. This could lead to the product being used past its expiration date. Stop using the product and follow the return/repair steps in the official notice.