AMSCORecalls & reported problems across all models
Corporation Steris Canada · 25 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
2 open recalls name at least one AMSCO model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 75
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls
- 2
We found 25 models of AMSCO by Corporation Steris Canada in the FDA's device registry (GUDID). Together they are named in 75 adverse event reports in the FDA's MAUDE database, received between Sep 28, 2017 and Sep 30, 2026 — classified as 3 injuries, 72 malfunctions.
The most frequently reported specific device problem is “Leak/Splash” (19 reports).
2 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
AMSCO recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Nov 19, 2025Class IIOpen, Classified
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
Z-0910-2026 · Root cause: Process control · names 3 of these models · Recall details · FDA record ↗
- Nov 19, 2025Class IIOpen, Classified
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users).
Z-0909-2026 · Root cause: Process control · names 3 of these models · Recall details · FDA record ↗
Most reported AMSCO problems
Device problems
- Leak/Splash19
- Use of Device Problem13
- Adverse Event Without Identified Device or Use Problem6
- Detachment of Device or Device Component6
- Improper or Incorrect Procedure or Method5
- Mechanical Jam5
- Insufficient Device Problem Information4
- Fire3
Patient problems
- No Clinical Signs, Symptoms or Conditions31
- Bruise/Contusion10
- Abrasion7
- Laceration(s)7
- Pain7
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available2
- Bone Fracture(s)2
- Damage to Ligament(s)2
AMSCO models
25 models, most reported first. Each model has its own page with its reports, recalls and device details.
- AMSCO 7052HPDisinfector, medical devices1 recall10 reports
- AMSCO 7053HPDisinfector, medical devices1 recall10 reports
- AMSCO 7052HPDisinfector, medical devices1 recall9 reports
- AMSCO 7053HPDisinfector, medical devices1 recall7 reports
- AMSCO 7052HPDisinfector, medical devices1 recall3 reports
- AMSCO 7053HPDisinfector, medical devices1 recall2 reports
- AMSCO 5052Disinfector, medical devices5 reports
- AMSCO 5052Disinfector, medical devices4 reports
- AMSCO 2532Disinfector, medical devices3 reports
- AMSCO 7053LDisinfector, medical devices2 reports
- AMSCO Drying CabinetEndoscope maintenance system2 reports
- AMSCO 7052HPDisinfector, medical devices2 reports
- AMSCO 5052Disinfector, medical devices2 reports
- AMSCO 7053LDisinfector, medical devices2 reports
- AMSCO 1215Disinfector, medical devices2 reports
- AMSCO 3052Disinfector, medical devices1 report
- AMSCO 5052Disinfector, medical devices1 report
- AMSCO 2532Disinfector, medical devices1 report
- AMSCO 2532Disinfector, medical devices1 report
- AMSCO 2532Disinfector, medical devices1 report
- AMSCO 3052Disinfector, medical devices1 report
- AMSCO 7053LDisinfector, medical devices1 report
- AMSCO 1215Disinfector, medical devices1 report
- AMSCO 1215Disinfector, medical devices1 report
- AMSCO Drying CabinetEndoscope maintenance system1 report
Recent AMSCO adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Leak/Splash
The user facility reported that their AMSCO 7052 HP Washer/Disinfector was leaking water.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946843 ↗MalfunctionSep 9, 2026Leak/Splash
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50696621 ↗MalfunctionSep 2, 2026Fire
The user facility reported that their AMSCO 2532 Single-Chamber Washer/Disinfector caught fire. The fire was extinguished by the fire department and the smoke was contained within the sterilizer. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50571263 ↗InjuryAug 13, 2026Mechanical Problem
Patient problems: Abrasion; Bruise/Contusion
MAUDE report 50239193 ↗InjuryJul 30, 2026Detachment of Device or Device Component
The user facility reported while an employee was cleaning their AMSCO 7053HP Washer/Disinfector the panel that cover's the facility's plumbing/water inlet adjacent to the unit detached and "struck" the employee on the arm. It is unknown if medical treatment was sought or administered.
Patient problems: Insufficient Information
MAUDE report 50082608 ↗InjuryJul 29, 2026Use of Device Problem
The user facility reported that an employee injured their hand while loading instrument racks into their AMSCO 7052HP Washer/Disinfector. The employee sought and received medical treatment at the facility's Emergency Room; however, it is unknown what medical treatment was administered.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50073943 ↗MalfunctionJul 9, 2026Improper or Incorrect Procedure or Method
Patient problems: Laceration(s)
MAUDE report 25771011 ↗MalfunctionJul 2, 2026Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY WHILE OPERATING A CART TO THEIR AMSCO 7053HP WASHER/DISINFECTOR. THE EMPLOYEE SOUGHT MEDICAL TREATMENT HOWEVER, IT IS UNKNOWN THE TREATMENT THAT MAY HAVE BEEN ADMINISTERED.
Patient problems: Pain
MAUDE report 25695394 ↗MalfunctionJun 9, 2026Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY TO THEIR HAND WHILE TRYING TO PUSH A CONTAINER BACK INTO THEIR AMSCO 5052 WASHER/DISINFECTOR WHILE THE DOOR WAS CLOSING. IT IS UNKNOWN IF THE EMPLOYEE SOUGHT OR RECEIVED MEDICAL TREATMENT.
Patient problems: Pain
MAUDE report 25447162 ↗MalfunctionMay 21, 2026Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT WHILE LOADING INSTRUMENTS FROM AN AMSCO 7053 HP WASHER/DISINFECTOR, THE WASHER DOOR CONTACTED AN EMPLOYEE'S HAND, RESULTING IN SCRATCHES. IT IS UNKNOWN IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Abrasion
MAUDE report 25244251 ↗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 ↗MalfunctionMay 1, 2026Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A SHOULDER BRUISE WHILE ATTEMPTING TO PUSH A RACK INTO TO THEIR AMSCO 7053 HP WASHER/DISINFECTOR. IT IS UNKNOWN IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Bruise/Contusion
MAUDE report 25060160 ↗MalfunctionApr 9, 2026Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT WHILE REMOVING INSTRUMENTS FROM AN AMSCO 7052 HP WASHER/DISINFECTOR, THE WASHER DOOR CONTACTED ON AN EMPLOYEE'S FOREARM, RESULTING IN A BRUISE. THE DOOR RETRACTED AFTER CONTACTING THE EMPLOYEE'S FOREARM, AND THE SAFETY BAR FUNCTIONED AS DESIGNED. MEDICAL TREATMENT WAS SOUGHT; HOWEVER, IT IS UNKNOWN WHAT MEDICAL TREATMENT WAS ADMINISTERED.
Patient problems: Bruise/Contusion
MAUDE report 24835638 ↗MalfunctionApr 1, 2026Detachment 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 AND CONTACTED THE EMPLOYEE'S HEAD. THE EMPLOYEE SOUGHT MEDICAL TREATMENT AND RECEIVED A CT SCAN WHICH CONFIRMED NO FURTHER INJURIES OR MEDICAL TREATMENT REQUIRED. THE EMPLOYEE RETURNED TO WORK.
Patient problems: Headache; Swelling/ Edema
MAUDE report 24760076 ↗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 AMSCO 7052 HP 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 24697986 ↗
Other Corporation Steris Canada products
All Corporation Steris Canada devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page