Skip to content

NA 0331000400Recalls & reported problems

Stryker Corporation · Right-Angle Adapter for Autoclavable Scopes · Class 2

Adverse event reports
3
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327057225), received between Nov 7, 2019 and May 4, 2023 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Temperature Problem” (3 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

Device problems

  • Temperature Problem3
  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Burn(s)2
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMay 4, 2023Temperature Problem; Temperature Problem

    IT WAS REPORTED THAT THERE WAS PATIENT BURN.

    Patient problems: Burn(s)

    MAUDE report 16868228 ↗
  • MalfunctionNov 5, 2020Temperature Problem

    IT WAS REPORTED THAT THERE WAS A THERMAL EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10794498 ↗
  • InjuryNov 7, 2019Temperature Problem; Adverse Event Without Identified Device or Use Problem; Temperature Problem

    IT WAS REPORTED THAT A PATIENT WAS BURNED.

    Patient problems: Burn(s)

    MAUDE report 9293294 ↗

Other Light source, fiberoptic, routine devices

All Light source, fiberoptic, routine devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.