InnerVision® 1465-50Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00816734021293), received between Jul 9, 2018 and Jan 15, 2019 — classified as 3 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJan 15, 2019Device Dislodged or Dislocated

  A 50F BOUGIE TIP BECAME DISLODGED FROM THE ILLUMINATION CORD IN THE PATIENT¿S ESOPHAGUS.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8253670 ↗
• InjuryAug 27, 2018Use of Device Problem; Use of Device Problem

  CUSTOMER REPORTED ON MW5078295 THE 50FR BOUGIE TIP BECAME DISLODGED FROM THE ILLUMINATION CORD IN THE PATIENT'S ESOPHAGUS.

  Patient problems: Laceration(s) of Esophagus

  MAUDE report 7820278 ↗
• InjuryJul 9, 2018Device Dislodged or Dislocated

  A 50F BOUGIE TIP BECAME DISLODGED FROM THE ILLUMINATION CORD IN THE PT'S ESOPHAGUS.

  Patient problems: No Code Available

  MAUDE report 7673391 ↗