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Reveal 00711770 (UDI 00816765012642)Recalls & 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 00816765012642), received between Feb 13, 2019 and Feb 13, 2019 — 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

  • 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.

  • MalfunctionFeb 13, 2019Detachment of Device or Device Component

    THE USER FACILITY REPORTED THAT A REVEAL DISTAL ATTACHMENT CAP DETACHED FROM THE ENDOSCOPE DURING PROCEDURAL USE. THE DEVICE WAS RETRIEVED, AND THERE WAS NO REPORTED HARM TO THE PATIENT OR USER.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 8336203 ↗

Other endoscopic irrigation/suction system devices

All endoscopic irrigation/suction system devices →

Sources and updates

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