Health product recall

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

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe