AMSCO Drying Cabinet (REF DCR100101)Recalls & reported problems
Corporation Steris Canada · The AMSCO Drying Cabinet, 29-inch with Pass Through delivers unrivaled precision with exact temperature control, timers for every shelf and HEPA filtration. · 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 00724995162610), received between Jan 15, 2025 and May 21, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Connection 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
- Connection Problem1
- Sharp Edges1
Patient problems
- Abrasion1
- Electric Shock1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2026Connection Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE RECEIVED A "LIGHT ELECTRIC SHOCK" WHILE CLEANING THEIR AMSCO DRYING CABINET. NO MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED AND THE EMPLOYEE CONTINUED WORKING.
Patient problems: Electric Shock
MAUDE report 25243225 ↗MalfunctionJan 15, 2025Sharp Edges; Sharp Edges
THE USER FACILITY REPORTED THAT THREE EMPLOYEES OBTAINED CUTS TO THEIR FINGER(S) WHEN LOADING A RACK INTO THEIR AMSCO DRYING CABINET. THE FIRST EMPLOYEE SELF-APPLIED DURABOND ON TWO OF THEIR FINGERS AND CONTINUED WORKING. THE SECOND EMPLOYEE WAS REPORTED TO HAVE FAINTED AND HIT THEIR HEAD. IT IS UNKNOWN WHETHER MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED FOR THE SECOND EMPLOYEE. NO INFORMATION WAS PROVIDED PERTAINING TO THE THIRD EMPLOYEE.
Patient problems: Abrasion
MAUDE report 21162133 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.