Public recall detail

Flowtriever Retrieval/Aspiration System

2023-01-26

medium
Recall Safety notice
Quick summary

Quick summary: Flowtriever Retrieval/Aspiration System. Date: 2023-01-26.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Flowtriever Retrieval/Aspiration System. Date: 2023-01-26.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandInari Medical, Inc.
ProductFlowtriever Retrieval/Aspiration System
IssueMedical devices - Performance
Recall classType II
IdentificationRA-72616

Affected products

ProductFlowtriever Retrieval/Aspiration System
Lot22100025 22100024 22100020 22100026
Model22‐101
Serial number22100025 22100024 22100020 22100026
DescriptionFlowtriever Retrieval/Aspiration System

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

What you should do

  • Manufacturer authorized healthcare professionals to stop using and to destroy affected devices.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Cardiovascular
CompaniesInari Medical, Inc. 6001 Oak Canyon, Irvine, California, United States, 92618
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-72616
Background{}
CompaniesInari Medical, Inc. 6001 Oak Canyon, Irvine, California, United States, 92618
AudiencesHealthcare
Source updated2023-01-26

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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