Reliance Vision Single Chamber (REF FH05042)Recalls & reported problems
Corporation Steris Canada · The Reliance Vision Single-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), theater shoes and other similar and related items found in healthcare facilities. · Class 2
All models of Reliance Vision (8)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00724995192648), received between Sep 22, 2022 and Mar 28, 2025 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Use of Device 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem3
- Smoking1
- Unintended Movement1
Patient problems
- Insufficient Information2
- Pain2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 28, 2025Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS MANUALLY PUSHING A RACK INTO THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR WHEN THE DOOR CAME DOWN AND CONTACTED THEIR HAND. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT (BANDAGE) FOLLOWING THE REPORTED EVENT.
Patient problems: Pain
MAUDE report 21724094 ↗MalfunctionJan 31, 2025Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED VIA MEDWATCH #(B)(4) THAT THE DOOR TO THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR "SLAMMED SHUT AFTER OBSTRUCTION WAS CLEARED."
Patient problems: Pain
MAUDE report 21286131 ↗MalfunctionMay 9, 2024Smoking; Smoking
THE USER FACILITY REPORTED THAT THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR WAS EMITTING SMOKE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19280643 ↗MalfunctionApr 12, 2023Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT DURING THE AUTOMATED LOAD PROCESS, A RACK WAS NOT COMPLETELY INSERTED INTO THEIR RELIANCE VISION SINGLE CHAMBER WASHER/DISINFECTOR. AN EMPLOYEE PUSHED THE RACK INTO THE CHAMBER, AND THE WASHER DOOR CAME DOWN ON THE EMPLOYEE'S FINGERS. MEDICAL TREATMENT WAS SOUGHT AND ADMINISTERED.
Patient problems: Insufficient Information
MAUDE report 16724708 ↗MalfunctionSep 22, 2022Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED AN EMPLOYEE EXPERIENCED AN INJURY TO THEIR HAND WHILE LOADING A RACK OF INSTRUMENTS INTO THE RELIANCE VISION SINGLE CHAMBER WASHER/DISINFECTOR. MEDICAL TREATMENT WAS SOUGHT. THE USER FACILITY DID NOT DISCLOSE IF MEDICAL TREATMENT WAS ADMINISTERED.
Patient problems: Insufficient Information
MAUDE report 15464766 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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