XPS Nexus™ 1894510Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00643169434134), received between Sep 17, 2019 and Sep 17, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjurySep 17, 2019Electrical /Electronic Property Problem; Electrical /Electronic Property Problem

  A HEALTH CARE PROVIDER REPORTED THAT THE DEVICE HAD BLOWN FUSES DURING THE PROCEDURE. THE PATIENT WAS UNDER ANESTHESIA WHEN THE ISSUE OCCURRED. THEY HAD TO ROLL THEM OUT AFTER THE EQUIPMENT BROKE DOWN. THE CASE WAS CANCELED AND RESCHEDULED FOR A LATER DATE.

  Patient problems: Oversedation

  MAUDE report 9075232 ↗