LimFlow Vector VT-US-23Recalls & reported problems
Inari Medical, Inc. · The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00850041730134), received between Oct 15, 2025 and Oct 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Dec 5, 2025Open, Classified
Incorrect expiration date
Z-1218-2026 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 15, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
ON (B)(6) 2025, DURING A LIMFLOW TRANSCATHETER ARTERIALIZATION OF DEEP VEINS (TADV) PROCEDURE THE MEDICAL TEAM HAD DIFFICULTY DELIVERING THE VECTOR TO THE STARTING POINT. THE NOSE CONE OF THE VECTOR DEVICE BROKE OFF ON THE WIRE. THE PHYSICIAN WAS ABLE TO PUSH THE NOSE CONE OUT WITH A BALLOON THROUGH THE DISTAL VENOUS ACCESS. THERE WAS NO INJURY, AND THE NOSE CONE WAS SUCCESSFULLY REMOVED. A SECOND VECTOR DEVICE WAS USED AND THE PROCEDURE WAS COMPLETED WITHOUT FURTHER ISSUES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23287785 ↗
Other Valvulotome devices
- HYDRO LeMaitre Valvulotome 1009-00Lemaitre Vascular, Inc. · Valvulotome71 reports
- Eze-Sit Valvulotome 94cmLemaitre Vascular, Inc. · Valvulotome2 reports
- Over-the-Wire LeMaitre Valvulotome 1005-00Lemaitre Vascular, Inc. · Valvulotome1 report
- Expandable LeMaitre Valvulotome 1000-90Lemaitre Vascular, Inc. · Valvulotome1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.