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Bagley REXMR-6LARecalls & reported problems

Gyrus ACMI, LLC · Bagley Self-Dilating Autoclavable Semi-Rigid Ureteroscope · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00821925007833), received between Dec 30, 2020 and Aug 28, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 1 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Break2
  • Material Twisted/Bent1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Patient Involvement1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 28, 2024Break; Break

    IT WAS REPORTED, THE URETEROSCOPE, 43CM EXHIBITED A BROKEN LENS. THE ISSUE OCCURRED DURING REPROCESSING. THERE WERE NO REPORTS OF PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 20084552 ↗
  • MalfunctionDec 30, 2020Break; Material Twisted/Bent; Break; Material Twisted/Bent

    IT WAS REPORTED THAT THE DEVICE DISTAL TIP WAS FOUND BENT, DAMAGED, BROKEN WITH A SHARP EDGE. THERE WERE NO FURTHER DETAILS PROVIDED REGARDING THE REPORTED EVENT. NO PATIENT INVOLVEMENT REPORTED. NO USER INJURY REPORTED.

    Patient problems: No Patient Involvement

    MAUDE report 11095822 ↗

Other Ureteroscope And Accessories, Flexible/Rigid devices

All Ureteroscope And Accessories, Flexible/Rigid devices →

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