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LimFlow Vector

Inari Medical, Inc. · Model VT-US-21 · UDI-DI 00850041730028

MGZ Prescription
10
510(k) clearances
131
Adverse events
6
Recalls
13
Facilities

Description

The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves

Recalls

DateFirmReason
2025-12-05LimFlow, Inc.Incorrect expiration date
2023-07-13LeMaitre Vascular, Inc.Burrs (molding flash) on the cutter may tear the harvested vien
2016-08-03LeMaitre Vascular, Inc.Wire which deploys the loop may be come detached at the handle causing the device to be inoperable
2016-08-03LeMaitre Vascular, Inc.Wire which deploys the loop may be come detached at the handle causing the device to be inoperable
2016-08-03LeMaitre Vascular, Inc.Wire which deploys the loop may be come detached at the handle causing the device to be inoperable
2014-09-08Instrumed International, Inc.The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and therefore, does not meet a

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.