Acufex Access Advanced Positioning Kits recall in Canada: Sterility issue
In plain language
This recall involves Acufex Access Advanced Positioning Kits sold in Canada. They are being recalled because they did not undergo the required sterilization process. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Acufex Access Advanced Positioning Kits
Model: 72205104
Lot: 5096788, 50971615, 50971617
Why this matters
Sterility issue
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: 5096788, 50971615, 50971617
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 72205104
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?
Sterility issue
What should consumers do?
Stop using the product immediately. 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. Sterility issue
When was this product recalled?
This product was recalled on December 21, 2021.
Is the Smith & Nephew, Inc., Endoscopy Division brand affected by this recall?
Yes, Smith & Nephew, Inc., Endoscopy Division products are affected by this recall. This recall involves Acufex Access Advanced Positioning Kits sold in Canada. They are being recalled because they did not undergo the required sterilization process. Stop using the product and contact the manufacturer for more information.