Reliance Vision Single Chamber (REF FH05072)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 00724995192686), received between Jan 3, 2024 and Apr 17, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (2 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
- Leak/Splash2
- Improper or Incorrect Procedure or Method1
- Mechanical Jam1
- Use of Device Problem1
Patient problems
- Bone Fracture(s)2
- No Clinical Signs, Symptoms or Conditions2
- Fall1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 17, 2026Improper or Incorrect Procedure or Method
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY (BROKEN FINGER) WHEN THE DOOR TO THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR CONTACTED THEIR HAND. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT AT THE FACILITY'S EMERGENCY ROOM.
Patient problems: Bone Fracture(s)
MAUDE report 24913264 ↗MalfunctionMar 26, 2026Use of Device Problem
WHILE ONSITE AT THE USER FACILITY, A STERIS INSTALLATION SPECIALIST OBSERVED THAT USER FACILITY PERSONNEL WERE USING A DETERGENT DURING CYCLES WHICH DID NOT ALIGN WITH THE DETERGENT PARAMETERS SET ON THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR. IT IS UNKNOWN HOW MANY INSTRUMENTS WERE PROCESSED WITH THIS DETERGENT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24698021 ↗MalfunctionNov 27, 2024Leak/Splash; Leak/Splash
THE USER FACILITY REPORTED THAT WATER WAS LEAKING FROM THEIR RELIANCE VISION-SINGLE CHAMBER WASHER/DISINFECTOR ONTO THE FLOOR. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20791843 ↗MalfunctionJan 25, 2024Leak/Splash; Leak/Splash
THE USER FACILITY REPORTED THAT THEIR RELIANCE VISION SINGLE-CHAMBER WASHER/DISINFECTOR WAS LEAKING WATER ONTO THE FLOOR CAUSING EMPLOYEES TO SLIP AND FALL RESULTING IN INJURIES. THE USER FACILITY DID NOT DISCLOSE WHAT MEDICAL TREATMENT WAS ADMINISTERED.
Patient problems: Fall
MAUDE report 18582587 ↗MalfunctionJan 3, 2024Mechanical Jam; Mechanical Jam
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A CUT AND BROKEN BONE ON THEIR HAND WHILE OPERATING THE RELIANCE VISION SINGLE CHAMBER WASHER/DISINFECTOR. MEDICAL TREATMENT SOUGHT AND ADMINISTERED.
Patient problems: Bone Fracture(s)
MAUDE report 18437100 ↗
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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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