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RELIANCE Reliance 6500 (REF REL650020MU)Recalls & reported problems

Steris Corporation · RELIANCE 6500 Series HEPA Filter Drying Cabinet, 20 Scope Main Unit is designed to help you manage access to your endoscope inventory, track key parameters, and easily access vertically hanging endoscopes, all in an organized and controlled drying environment. · 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 00724995229511), received between Oct 17, 2025 and May 15, 2026 — classified as 2 malfunctions.

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

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: 0 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: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 1 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

  • Break1
  • Sharp Edges1

Patient problems

  • Abrasion1
  • Insufficient Information1
  • Laceration(s)1

Recent adverse event reports

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

  • MalfunctionMay 15, 2026Break

    THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED CUTS AFTER THE TEMPERED GLASS DOOR TO THEIR RELIANCE 6500 ENDOSCOPE DRYING AND STORAGE CABINET "SHATTERED." THE EMPLOYEE RECEIVED MEDICAL TREATMENT, HOWEVER IT IS UNKNOWN WHAT TYPE OF MEDICAL TREATMENT WAS ADMINISTERED.

    Patient problems: Abrasion

    MAUDE report 25183945 ↗
  • MalfunctionOct 17, 2025Sharp Edges; Sharp Edges

    THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY FROM THE SHARP EDGES OF THE DRIP PAN OF THEIR 6500 SERIES HEPA DRYING CABINET. THE EMPLOYEE DID NOT SEEK MEDICAL TREATMENT AND CONTINUED WORKING.

    Patient problems: Insufficient Information; Laceration(s)

    MAUDE report 23324610 ↗

Other Endoscope maintenance system devices

All Endoscope maintenance system devices →

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