NA 0502740061Recalls & reported problems
Stryker Corporation · Hysteroscope Operative Sheath (Inner) · 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 07613327059977), received between Sep 29, 2020 and Sep 29, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fitting 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Fitting Problem1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2020Fitting Problem; Fitting Problem
IT WAS REPORTED THAT THERE WAS A SURGICAL DELAY OF MORE THAN 30 MINUTES.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 10602705 ↗
Other EVACUATOR, GASTRO-UROLOGY devices
- AHTO 0250070600Stryker Corporation · EVACUATOR, GASTRO-UROLOGY2 recalls44 reports
- Gyrus ACMI 190AGyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY2 recalls0 reports
- Toomey 188Gyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Toomey 188AGyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- USA Elite 191-NRSGyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Gyrus ACMI 190-4Gyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Gyrus ACMI 194-2Gyrus ACMI, LLC · EVACUATOR, GASTRO-UROLOGY1 recall0 reports
- Bard® Ellik Evacuator 000451C. R. Bard, Inc. · EVACUATOR, GASTRO-UROLOGY42 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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