MultiTASC Dissection/Transection Device 4500-05Recalls & reported problems
Lemaitre Vascular, Inc. · MultiTASC Dissection/Transection Device, 7mm · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840663105847), received between Jan 25, 2018 and Jan 25, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Bent” (1 report).
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.
Most reported problems
Device problems
- Bent1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 25, 2018Bent; Bent
DURING REMOTE ENDARTERECTOMY, WHILE DISSECTING AN ATHEROMATOUS CORE FROM THE VESSEL WALL IN THE SFA, PHYSICIAN NOTICED THAT THE HANDLE NEAR THE RING HAD BENT. SURGEON HAD TO EXTEND THE ARTERIOTOMY TO GAIN ACCESS TO THE CORE SINCE IT WAS PUSHED DOWN.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7219909 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.