Ascenda Intrathecal Catheters recall in Canada: Performance issue
In plain language
This recall involves Ascenda Intrathecal Catheters and Ascenda Intrathecal Catheter Pump Segment Revision Kits sold in Canada. They are being recalled due to a design update to reduce the potential for tissue growth, which could lead to catheter occlusion. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Ascenda Intrathecal Catheter
Model: 8780, 8781
Lot: More than 10 numbers, contact manufacturer.
Ascenda Intrathecal Catheter Pump Segment Revision Kit
Model: 8784
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Catheter occlusion
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: 8780, 8781, 8784
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?
Catheter occlusion
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. Catheter occlusion
When was this product recalled?
This product was recalled on May 28, 2024.
Is the MEDTRONIC INC. brand affected by this recall?
Yes, MEDTRONIC INC. products are affected by this recall. This recall involves Ascenda Intrathecal Catheters and Ascenda Intrathecal Catheter Pump Segment Revision Kits sold in Canada. They are being recalled due to a design update to reduce the potential for tissue growth, which could lead to catheter occlusion. Healthcare professionals should contact the manufacturer for more information.