Revitan Modular Rasp recall in Canada: potential breakage during surgery
In plain language
This recall involves Revitan Modular Rasp Distal Curved and Revitan Rasp Distal Curved medical devices sold in Canada. They are being recalled because they may break during surgery after extensive use. Healthcare professionals should stop using the affected products and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check model numbers against the recall notice.
- Contact the manufacturer for return or replacement instructions.
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Affected products
Revitan Modular Rasp, Distal Curved
Model: 01.00409.612, 01.00409.613, 01.00409.614, 01.00409.617, 01.00409.622, 01.00409.623, 01.00409.624, 01.00409.625, 01.00409.626, 01.00409.627, 01.00409.628, 01.00409.629, 01.00409.633, 01.00409.634, 01.00409.635, 01.00409.636, 01.00409.637, 01.00409.638, 01.00409.639
Lot: More than 10 numbers, contact manufacturer.
Revitan Rasp Distal Curved
Model: 01.00409.612, 01.00409.613, 01.00409.614
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Potential breakage during surgery
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: 01.00409.612, 01.00409.613, 01.00409.614, 01.00409.617, 01.00409.622, 01.00409.623, 01.00409.624, 01.00409.625, 01.00409.626, 01.00409.627, 01.00409.628, 01.00409.629, 01.00409.633, 01.00409.634, 01.00409.635, 01.00409.636, 01.00409.637, 01.00409.638, 01.00409.639
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?
Potential breakage during surgery
What should consumers do?
Stop using the product immediately. Check model numbers against the recall notice. Contact the manufacturer for return or replacement 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?
Yes, there may be a health risk. Potential breakage during surgery
When was this product recalled?
This product was recalled on January 29, 2018.
Is the Revitan brand affected by this recall?
Yes, Revitan products are affected by this recall. This recall involves Revitan Modular Rasp Distal Curved and Revitan Rasp Distal Curved medical devices sold in Canada. They are being recalled because they may break during surgery after extensive use. Healthcare professionals should stop using the affected products and follow the return steps in the official notice.