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Reliance Vision Multi-Chamber (REF FH83062)Recalls & reported problems

Corporation Steris Canada · The Reliance Vision Multi-Chamber Washer Disinfector Steam Unit is intended for use in the cleaning and intermediate level disinfection of soiled reusable utensils, trays, glassware, bedpans and urinals, rubber and plastic goods, simple hard-surfaced rigid surgical instruments (such as forceps and clamps) and other related articles found in healthcare facilities. · Class 2

Adverse event reports
4
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00724995193171), received between Jun 1, 2023 and Jul 16, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Application Program Problem” (3 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. 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: 2 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 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: 1 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Application Program Problem3
  • Insufficient Device Problem Information1
  • Use of Device Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions3
  • Bruise/Contusion1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 16, 2026Use of Device Problem

    Patient problems: Bruise/Contusion

    MAUDE report 25844858 ↗
  • MalfunctionMar 30, 2025Application Program Problem; Application Program Problem

    THE USER FACILITY REPORTED VIA VIGILANCE REPORT THAT THEIR RELIANCE VISION MULTI-CHAMBER WASHER/DISINFECTOR EXPERIENCED A "DIGITAL PRINTOUT PROBLEM". NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21728759 ↗
  • MalfunctionMar 30, 2025Application Program Problem; Application Program Problem

    THE USER FACILITY REPORTED VIA VIGILANCE REPORT THAT THEIR RELIANCE VISION MULTI-CHAMBER WASHER/DISINFECTOR EXPERIENCED A "DIGITAL PRINTOUT PROBLEM". NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 21728756 ↗
  • MalfunctionJun 1, 2023Application Program Problem; Insufficient Device Problem Information; Application Program Problem; Insufficient Device Problem Information

    THE USER FACILITY REPORTED VIA VIGILANCE REPORT THAT THEIR RELIANCE VISION MULTI-CHAMBER WASHER/DISINFECTOR IS EXPERIENCING A "COMPUTER SOFTWARE PROBLEM". NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17037701 ↗

Other Disinfector, medical devices devices

All Disinfector, medical devices devices →

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