RELIANCE Reliance 6500 Connectors (REF RELTSO100BRONCH)Recalls & reported problems
Steris Corporation · The OLYMPUS 160/180/190 BRONCHOSCOPE Tube Set is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00724995229696), received between Aug 17, 2026 and Aug 26, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component2
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.
MalfunctionAug 26, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50452068 ↗MalfunctionAug 17, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50287741 ↗
Other Endoscope maintenance system devices
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system5 reports
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system4 reports
- RELIANCE Reliance 6500Steris Corporation · Endoscope maintenance system3 reports
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system2 reports
- ENDODRY Storage and Drying CabinetCantel Medical (Italy) Srl · Endoscope maintenance system2 reports
- RELIANCE Reliance 6500Steris Corporation · Endoscope maintenance system2 reports
- AMSCO Drying CabinetCorporation Steris Canada · Endoscope maintenance system2 reports
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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