Duet External Drainage And Monitoring Systems
Brand(s)
Last updated
Summary
Product
Duet External Drainage And Monitoring Systems
Issue
Medical devices - Performance
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 |
|---|---|---|
| Duet External Drainage And Monitoring System, Interlink Injection Sites, Ventricular | More than 10 numbers, contact manufacturer. | 46915 |
| Duet External Drainage And Monitoring System, Smartsite Injection Sites, Ventricular Catheter | More than 10 numbers, contact manufacturer. | 46916 |
| Duet External Drainage And Monitoring System, Smartsite Injection Sites | More than 10 numbers, contact manufacturer. | 46913 |
| Duet External Drainage And Monitoring System, Interlink Injection Sites, Lumbar Catheter | 223999040 224301720 226756273 | 46917 |
| Duet External Drainage And Monitoring System, Interlink Injection Sites | More than 10 numbers, contact manufacturer. | 46914 |
Issue
Medtronic is recalling Duet External Drainage and Monitoring System (EDMS) products due to the potential catheter disconnection from the patient line stopcock connectors.
Recall start date: January 23, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
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-75067
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