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USA Elite EMRS-24Recalls & reported problems

Gyrus ACMI, LLC · USA Elite System Standard Metal Resectoscope Sheath · Class 2

All models of USA Elite (24)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00821925001961), received between Jul 28, 2022 and May 17, 2023 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

7 other recalls cover devices cleared under the same FDA submission (K890328); they may or may not involve this specific model.

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 18, 2026.

Most reported problems

Device problems

  • Break1
  • Detachment of Device or Device Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

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

  • InjuryMay 17, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    A COMPANY REPRESENTATIVE, ON BEHALF OF A USER FACILITY, REPORTED THAT THE TIP OF THE NON-CF RESECTOSCOPE METAL SHEATH, 24 FR FELL OFF IN THE PATIENT AND WAS NOT RETRIEVED DUE TO CONCERN ABOUT TEARING THE URETER. THE PATIENT WAS ADMITTED FOR OBSERVATION. ADDITIONAL INFORMATION WAS REQUESTED MULTIPLE TIMES REGARDING THE OUTCOME AND OTHER EVENT DETAILS, BUT WAS NOT RECEIVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16945540 ↗
  • MalfunctionJul 28, 2022Break; Break

    A USER FACILITY REPORTED THAT THE DISTAL TIP OF A SCOPE WAS BROKEN. IT IS UNKNOWN WHEN THE REPORTED ISSUE OCCURRED. THERE WAS NO PATIENT INJURY OR ADVERSE EVENT REPORTED TO OLYMPUS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15123177 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K890328. One submission often covers many models, so check the product and lot details in each record.

  • Z-3299-2026 · Aug 24, 2026 · Open, Classified
    Olympus M3 Gold Autoclavable Foroblique Telescope 30. Model Number: M3-30A.
  • Z-3300-2026 · Aug 24, 2026 · Open, Classified
    Olympus M3 Gold Autoclavable Lateral Telescope 70. Model Number: M3-70A.
  • Z-2720-2026 · May 5, 2026 · Open, Classified
    Olympus Ellik Evacuator Includes Glass Body, Male Connecting Tubing & Latex Bulb. Model Number: 194.
  • Z-2139-2025 · Jun 18, 2025 · Open, Classified
    Blue Silicone, Reusable Silicone Seal 6 - 12 FR. Model Number: CS-B612. The reusable silicone seals fit over the biopsy port of endoscopes to seal off the working channel. Some
  • Z-2140-2025 · Jun 18, 2025 · Open, Classified
    Green Silicone Seal for Accessories, Reusable Silicone Seal 0 - 7 FR. Model Number: CS-G7. The reusable silicone seals fit over the biopsy port of endoscopes to seal off the work
  • Z-0568-2024 · Oct 2, 2023 · Open, Classified
    ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting Loop Electrode Stabilized, 0.012 Wire 24 Fr (8mm), Model: REF M
  • Z-1952-2018 · Apr 17, 2018 · Terminated
    Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists of a single conductor stranded wire terminated with plugs t

Other Hysteroscope (And Accessories) devices

All Hysteroscope (And Accessories) devices →

Sources and updates

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