REGENEREX PRIMARY TAPER recall in Canada: not properly sterilized
In plain language
This recall involves REGENEREX PRIMARY TAPER medical devices sold in Canada. They are being recalled because they may not have been properly sterilized. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check lot or serial numbers.
- Return the affected products as instructed.
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Affected products
REGENEREX PRIMARY TAPER
Model: 141269
Lot: 23900, 58930, 200720, 313260, 324440, 389060, 997610
Why this matters
Risk of infection due to improper sterilization
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: 23900, 58930, 200720, 313260, 324440, 389060, 997610
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 141269
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?
Risk of infection due to improper sterilization
What should consumers do?
Stop using the product immediately. Check lot or serial numbers. Return the affected products as instructed.
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. Risk of infection due to improper sterilization
When was this product recalled?
This product was recalled on September 25, 2020.
Is the REGENEREX brand affected by this recall?
Yes, REGENEREX products are affected by this recall. This recall involves REGENEREX PRIMARY TAPER medical devices sold in Canada. They are being recalled because they may not have been properly sterilized. Stop using the product and follow the return steps in the official notice.