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Edge SD303BARecalls & reported problems

Covidien LP · Bronchoscope Adapter;For use with Olympus 190 bronchoscopes · Class 2

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521199545), received between May 14, 2020 and May 14, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Application Program 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Application Program Problem1
  • Component or Accessory Incompatibility1

Patient problems

  • No Code Available1

Recent adverse event reports

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

  • InjuryMay 14, 2020Application Program Problem; Component or Accessory Incompatibility; Application Program Problem; Component or Accessory Incompatibility

    ACCORDING TO THE REPORTER, DURING THE PROCEDURE, THE SURGEON WAS UNABLE TO PASS THE CABLE THRU PORT. THE PROCEDURE WAS NOT COMPLETED.

    Patient problems: No Code Available

    MAUDE report 10058246 ↗

Other System, x-ray, tomography, computed devices

All System, x-ray, tomography, computed devices →

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