Vision Multi-ChamberRecalls & reported problems
Corporation Steris Canada · The Vision Multi-Chamber Washer Disinfector 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
- 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 00724995193140), received between Mar 21, 2025 and Mar 21, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device Problem” (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
- Use of Device Problem1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 21, 2025Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT THEIR VISION MULTI-CHAMBER WASHER DISINFECTOR DISPLAYED AN ERROR MESSAGE INDICATING THE DOOR WAS NOT CLOSING. AS THE EMPLOYEE PROCEEDED TO ADJUST THE INSTRUMENT RACK INSIDE THE WASHER, THE DOOR LOWERED AND CONTACTED THE EMPLOYEE'S HAND. THE EMPLOYEE SOUGHT TREATMENT AT THE ER; HOWEVER, IT IS UNKNOWN WHAT TREATMENT THE EMPLOYEE MAY HAVE RECEIVED.
Patient problems: Pain
MAUDE report 21663729 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.