Consumer product recall in Canada: Double Blade Shoe F/Unigraft Knife
In plain language
This recall involves the Double Blade Shoe F/Unigraft Knife 1.5 Thick x 9mm sold in Canada. It's being recalled because the product inside the package is incorrect; a single blade shoe was mistakenly packaged instead of a double blade shoe. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check lot number M050225.
- Contact ACE Surgical Supply Inc. for return instructions.
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Affected products
Double Blade Shoe F/Unigraft Knife 1.5 Thick x 9mm
Model: 6500009
Lot: M050225
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: M050225
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 6500009
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 the Double Blade Shoe F/Unigraft Knife 1.5 Thick x 9mm sold in Canada. It's being recalled because the product inside the package is incorrect; a single blade shoe was mistakenly packaged instead of a double blade shoe. Stop using the product and follow the return steps in the official notice.
What should consumers do?
Stop using the product immediately. Check lot number M050225. Contact ACE Surgical Supply Inc. for return instructions.
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 June 6, 2018.