Regeneten Tendon Anchors recall in Canada: Sterility issue
In plain language
This recall involves Regeneten Tendon Anchors (8) sold in Canada. They are being recalled because of a potential sterility issue due to packaging. This could lead to contamination of the sterile product. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Regeneten Tendon Anchors (8)
Model: 72205201
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Contamination risk due to 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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 72205201
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?
Contamination risk due to sterility issue
What should consumers do?
Contact the manufacturer if you require 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. Contamination risk due to sterility issue
When was this product recalled?
This product was recalled on August 29, 2024.
Is the Smith & Nephew, Inc. Endoscopy brand affected by this recall?
Yes, Smith & Nephew, Inc. Endoscopy products are affected by this recall. This recall involves Regeneten Tendon Anchors (8) sold in Canada. They are being recalled because of a potential sterility issue due to packaging. This could lead to contamination of the sterile product. Contact the manufacturer for more information.