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Reliance 6000 Series (REF REC6102DS)Recalls & reported problems

Corporation Steris Canada · The 6000 Series Reliance Endoscope Drying and Storage Cabinet, 10 Scopes (requires connectors) is designed to ensure a clean storage location for disinfected endoscopes and to protect the endoscopes from damage while in storage. · 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 00724995168100), received between Jul 17, 2025 and Jul 17, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Sharp Edges” (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: 1 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 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

  • Sharp Edges1

Patient problems

  • Laceration(s)1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 17, 2025Sharp Edges; Sharp Edges

    THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS CLEANING THE CHAMBER OF THEIR RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET AND OBTAINED A SMALL CUT TO THEIR HAND. THE EMPLOYEE DID NOT SEEK OR RECEIVE MEDICAL TREATMENT AND CONTINUED WORKING.

    Patient problems: Laceration(s)

    MAUDE report 22529487 ↗

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.