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Reveal 00711772Recalls & reported problems

US Endoscopy · The Reveal distal attachment cap is attached to the distal end of the endoscope to facilitate endoscopic therapy. The Reveal distal attachment cap is intended for the following: gastrointestinal mucosal resection (endoscopic mucosal resection) and keeping the suitable depth of endoscope's view field. · Class 2

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00816765012680), received between Sep 26, 2018 and Sep 26, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 16, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • Foreign Body In Patient1

Recent adverse event reports

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

  • MalfunctionSep 26, 2018Detachment of Device or Device Component

    THE USER FACILITY REPORTED THAT A REVEAL DISTAL ATTACHMENT CAP DETACHED FROM THE SCOPE IN THE PATIENT'S ESOPHAGUS DURING PROCEDURAL USE. THE DEVICE WAS RETRIEVED, THE PROCEDURE WAS COMPLETED, AND THERE WAS NO REPORTED HARM TO THE PATIENT OR USER OF THE DEVICE.

    Patient problems: Foreign Body In Patient

    MAUDE report 7911400 ↗

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Sources and updates

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