Bipolar Hugo RAS Systems
In plain language
This recall involves Bipolar Hugo RAS Systems sold in Canada. They are being recalled because a component failure could lead to uncontrolled instrument motion during surgery. Healthcare professionals should stop using the affected instruments and contact the manufacturer for more information.
What to do
- Stop using the affected instruments immediately.
- Check the model numbers provided in the official notice.
- Contact the manufacturer for additional information.
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Affected products
Hugo RAS Bipolar Maryland Forceps
Model: MRASI0005
Lot: More than 10 numbers, contact manufacturer.
Hugo RAS Bipolar Fenestrated Grasper
Model: MRASI0004
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Uncontrolled motion 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: MRASI0004, MRASI0005
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?
Uncontrolled motion during surgery
What should consumers do?
Stop using the affected instruments immediately. Check the model numbers provided in the official notice. 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. Uncontrolled motion during surgery
When was this product recalled?
This product was recalled on February 19, 2026.
Is the COVIDIEN LLC brand affected by this recall?
Yes, COVIDIEN LLC products are affected by this recall. This recall involves Bipolar Hugo RAS Systems sold in Canada. They are being recalled because a component failure could lead to uncontrolled instrument motion during surgery. Healthcare professionals should stop using the affected instruments and contact the manufacturer for more information.