Reliance Vision Single Chamber (REF FH05043)Recalls & reported problems
Corporation Steris Canada · The Reliance Vision Single-Chamber Washer Disinfector, Electric 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
- 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 00724995192655), received between Apr 12, 2023 and Jul 18, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
- Unintended Movement1
- Use of Device Problem1
Patient problems
- Bruise/Contusion1
- 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.
MalfunctionJul 18, 2025Unintended Movement; Insufficient Device Problem Information; Unintended Movement; Insufficient Device Problem Information
THE USER FACILITY REPORTED AN EMPLOYEE WAS INJURED WHILE USING THEIR RELIANCE VISION-SINGLE CHAMBER WASHER/DISINFECTOR. NO FURTHER DETAILS HAVE BEEN PROVIDED AT THIS TIME
Patient problems: Bruise/Contusion; Insufficient Information
MAUDE report 22540616 ↗MalfunctionApr 12, 2023Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS MANUALLY REMOVING AN OBSTRUCTION FROM THEIR RELIANCE VISION-SINGLE CHAMBER WASHER/DISINFECTOR WHEN THE CHAMBER DOOR CAME DOWN AND CONTACTED THE EMPLOYEE'S HAND; THE EMPLOYEE OBTAINED A CUT. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT.
Patient problems: Laceration(s)
MAUDE report 16727201 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.