Integra® 3714040Recalls & reported problems
Integra Lifesciences Production Corporation · Integra® Woodson Elevator · Class 1
- 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 10381780078012), received between Jul 18, 2025 and Jul 18, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionJul 18, 2025Break; Break
A FACILITY REPORTED THAT THE ELEVATOR 3714040 WOODSON DBL 10/30DEG (3714040) BROKE OFF IN THE PATIENT'S NOSE DURING A CLOSED REDUCTION NASAL FRACTURE PROCEDURE. THE BROKEN PIECE WAS RETRIEVED FROM THE NOSE WITHOUT ANY COMPLICATIONS RELATED TO THE BROKEN ELEVATOR. ANOTHER INSTRUMENT WAS USED TO COMPLETE THE SURGERY. NO INJURIES, OR DEATH, BUT AN ADDITIONAL FIVE-MINUTE DELAY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22542348 ↗
Other ELEVATOR, ENT devices
- Integra® Miltex® 22-302Integra Lifesciences Production Corporation · ELEVATOR, ENT2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.