Flowtriever Retrieval/Aspiration System
Brand(s)
Last updated
Summary
Product
Flowtriever Retrieval/Aspiration System
Issue
Medical devices - Performance issue
What to do
Manufacturer authorized healthcare professionals to stop using and to destroy affected devices.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Flowtriever Retrieval/Aspiration System |
22100025 |
22‐101 |
Issue
There is a potential malfunction with the side-port of the Triever 24. The side-port may potentially leak or dislodge during device preparation or during actual use. The side-port of the triever24 catheter is used in combination with a 60cc large bore syringe to facilitate aspiration of thrombotic material.
Recall start date: December 30, 2022
Additional information
Details
Original published date: 2023-01-26
Alert / recall type
Health product recall
Category
Health product - Medical device - Cardiovascular
Companies
Inari Medical, Inc.
6001 Oak Canyon, Irvine, California, United States, 92618
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-72616