Ascenda Intrathecal Catheters
Brand(s)
Last updated
Summary
Product
Ascenda Intrathecal Catheters
Issue
Medical devices - Performance issue
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
Ascenda Intrathecal Catheter |
More than 10 numbers, contact manufacturer. |
8780 |
Ascenda Intrathecal Catheter Pump Segment Revision Kit |
More than 10 numbers, contact manufacturer. |
8784 |
Issue
Medtronic is notifying customers of a design update implemented to reduce the potential for tissue growth into the Ascenda™ catheter connector which may potentially lead to catheter occlusion.
Recall start date: May 15, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
| Medtronic Inc. |
| 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75575
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