RELIANCE Reliance 6500 Connectors (REF RELTSOEBUS)Recalls & reported problems
Steris Corporation · The OLYMPUS EBUS BRONCHOSCOPE Tube Set is used with the Reliance 6500 Series Endoscope Drying and Storage Cabinet. · Class 2
- 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 00724995229719), received between Aug 17, 2026 and Aug 17, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- 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.
MalfunctionAug 17, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50287759 ↗
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
- ENDODRY Storage and Drying CabinetCantel Medical (Italy) Srl · Endoscope maintenance system2 reports
- RELIANCE Reliance 6500Steris Corporation · Endoscope maintenance system2 reports
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system2 reports
- RELIANCE Reliance 6500 ConnectorsSteris Corporation · Endoscope maintenance system2 reports
- AMSCO Drying CabinetCorporation Steris Canada · Endoscope maintenance system2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.