AMSCO 1215 (REF FW12102)Recalls & reported problems
Corporation Steris Canada · AMSCO 1215 Cart and Utensil Washer/Disinfector, 460-480V, 60hz, Steam Heated has a small footprint that maximizes experiences by significantly reducing manual cleaning of case carts and containers. · 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 00724995214401), received between May 9, 2024 and Mar 6, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component2
Patient problems
- Abrasion1
- Bruise/Contusion1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 6, 2026Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT WHILE AN EMPLOYEE WAS LOADING A CART INTO THEIR AMSCO 1215 CART AND UTENSIL WASHER/DISINFECTOR, THE TOP PANEL OF THE UNIT DETACHED AND CONTACTED HER HEAD AND FACE. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT.
Patient problems: Abrasion
MAUDE report 24532905 ↗MalfunctionMay 9, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT WHILE AN EMPLOYEE WAS LOADING THEIR AMSCO 1215 CART & UTENSIL WASHER/DISINFECTOR, THE TOP PANEL FELL OFF AND HIT THE EMPLOYEE IN THE FOREHEAD. THE EMPLOYEE SOUGHT AND RECEIVED MEDICAL TREATMENT AND RETURNED TO WORK.
Patient problems: Bruise/Contusion
MAUDE report 19280299 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.