RelianceRecalls & reported problems across all models
Corporation Steris Canada · 8 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 20
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 1
We found 8 models of Reliance by Corporation Steris Canada in the FDA's device registry (GUDID). Together they are named in 20 adverse event reports in the FDA's MAUDE database, received between Mar 9, 2022 and Jul 31, 2026 — classified as 2 injuries, 18 malfunctions.
The most frequently reported specific device problem is “Sharp Edges” (9 reports).
1 FDA recall record name at least one of these models by its device identifier.
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
Reliance 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.
- Apr 22, 2022Class IITerminated
The firm identified that when the electrical contactor component in the drying chamber of the Washer/Disinfector malfunctions, the heating elements in the drying chamber could overheat, eventually resulting in smoke and/or fire.
Z-1256-2022 · Root cause: Component design/selection · Recall details · FDA record ↗
Most reported Reliance problems
Device problems
- Sharp Edges9
- Insufficient Device Problem Information8
- Use of Device Problem4
- Device Alarm System1
- Device Emits Odor1
- Display or Visual Feedback Problem1
- Improper or Incorrect Procedure or Method1
- Leak/Splash1
Patient problems
- Laceration(s)11
- No Clinical Signs, Symptoms or Conditions5
- Abrasion1
- Aspiration/Inhalation1
- Bruise/Contusion1
- Eye Irritation1
- Insufficient Information1
Reliance models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Reliance SynergyDisinfector, medical devices1 recall0 reports
- Reliance 6000 SeriesEndoscope maintenance system5 reports
- Reliance 1227Disinfector, medical devices5 reports
- Reliance 6000 SeriesEndoscope maintenance system4 reports
- Reliance 6000 SeriesEndoscope maintenance system2 reports
- Reliance 1227Disinfector, medical devices2 reports
- Reliance EPSAccessories, germicide, cleaning, for endoscopes1 report
- Reliance 6000 SeriesEndoscope maintenance system1 report
Recent Reliance adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryJul 31, 2026Insufficient Device Problem Information
The user facility reported that employees sustained cuts to their arms while loading and unloading endoscopes from their 6000 Series Reliance Endoscope Drying and Storage Cabinet. It is unknown whether medical treatment was sought or administered.
Patient problems: Laceration(s)
MAUDE report 50097902 ↗InjuryJul 31, 2026Insufficient Device Problem Information
The user facility reported that employees sustained cuts to their arms while loading and unloading endoscopes from their 6000 Series Reliance Endoscope Drying and Storage Cabinet. It is unknown whether medical treatment was sought or administered.
Patient problems: Laceration(s)
MAUDE report 50097562 ↗MalfunctionDec 19, 2025Display or Visual Feedback Problem; Display or Visual Feedback Problem
THE USER FACILITY REPORTED VIA MEDWATCH REPORT #(B)(4) THAT "COMPUTER ON THE CART WASHER SUFFERED AN ERROR BELIEVED TO BE A FAILING HARD DRIVE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23850381 ↗MalfunctionDec 11, 2025Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT WHEN THE DOOR TO THEIR RELIANCE 1227 CART AND UTENSIL WASHER/DISINFECTOR WAS OPENED FOLLOWING A COMPLETED CYCLE, STEAM AND VAPOR CAME OUT CAUSING THE FACILITY'S SPRINKLER SYSTEM TO BE SET OFF. PATIENT PROCEDURES WERE SUBSEQUENTLY POSTPONED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23780831 ↗MalfunctionJul 17, 2025Sharp Edges; Sharp Edges
THE USER FACILITY REPORTED THAT AN EMPLOYEE WAS CLEANING THE CHAMBER OF THEIR RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET AND OBTAINED A SMALL CUT TO THEIR HAND. THE EMPLOYEE DID NOT SEEK OR RECEIVE MEDICAL TREATMENT AND CONTINUED WORKING.
Patient problems: Laceration(s)
MAUDE report 22529487 ↗MalfunctionMar 21, 2025Use of Device Problem; Improper or Incorrect Procedure or Method; Use of Device Problem; Improper or Incorrect Procedure or Method
THE USER FACILITY REPORTED THAT EMPLOYEES EXPERIENCED INHALATION AND EYE IRRITATION DURING A CYCLE FOR THEIR RELIANCE 1227 CART AND UTENSIL WASHER DISINFECTOR. THE EMPLOYEES SOUGHT TREATMENT AT THE FACILITY'S EMERGENCY ROOM; HOWEVER, IT IS UNKNOWN WHAT TREATMENT MAY HAVE BEEN RECEIVED.
Patient problems: Aspiration/Inhalation; Eye Irritation
MAUDE report 21660320 ↗MalfunctionSep 12, 2024Sharp Edges; Sharp Edges
THE USER FACILITY REPORTED AN EMPLOYEE RECEIVED A SMALL CUT ON HER HAND WHILE CLEANING THEIR 6000 SERIES RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. THE EMPLOYEE SELF-ADMINISTERED A BANDAGE AND CONTINUED WORKING.
Patient problems: Laceration(s)
MAUDE report 20199974 ↗MalfunctionSep 12, 2024Sharp Edges; Sharp Edges
THE USER FACILITY REPORTED AN EMPLOYEE RECEIVED A SMALL CUT ON HER HAND WHILE CLEANING THEIR 6000 SERIES RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. THE EMPLOYEE SELF-ADMINISTERED A BANDAGE AND CONTINUED WORKING.
Patient problems: Laceration(s)
MAUDE report 20199973 ↗MalfunctionAug 15, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT TWO EMPLOYEES RECEIVED INJURIES FROM "SHARP EDGES" WHILE WIPING DOWN A 6000 SERIES ENDO DRYING CABINET. THE FIRST USER SUFFERED A MINOR LACERATION ON HER FINGER AND RECEIVED A BANDAGE FROM A MEDICAL PROFESSIONAL. THE SECOND SUFFERED A CUT ON THE BACK OF HER HAND AND RECEIVED STERI-STRIPS FROM A MEDICAL PROFESSIONAL.
Patient problems: Laceration(s)
MAUDE report 19995929 ↗MalfunctionMay 10, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE'S ARM WAS BRUISED FROM CLOSING A RELIANCE 1227 CART AND UTENSIL WASHER DOOR WHILE UNLOADING A SECOND CART. NO MEDICAL TREATMENT WAS SOUGHT.
Patient problems: Bruise/Contusion
MAUDE report 19286822 ↗MalfunctionFeb 28, 2024Insufficient Device Problem Information; Sharp Edges; Insufficient Device Problem Information; Sharp Edges
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A LACERATION TO THEIR HAND WHILE CLEANING THEIR RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. IT IS UNKNOWN IF THE EMPLOYEE SOUGHT OR RECEIVED MEDICAL TREATMENT.
Patient problems: Laceration(s)
MAUDE report 18804340 ↗MalfunctionFeb 27, 2024Insufficient Device Problem Information; Sharp Edges; Insufficient Device Problem Information; Sharp Edges
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A LACERATION TO THEIR HAND WHILE CLEANING THEIR RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. THE EMPLOYEE ELECTED NOT TO SEEK OR RECEIVE MEDICAL TREATMENT HOWEVER, SELF-TREATMENT WAS ADMINISTERED.
Patient problems: Laceration(s)
MAUDE report 18788909 ↗MalfunctionFeb 8, 2024Sharp Edges; Sharp Edges
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED A CUT ON THEIR HAND WHILE CLEANING THEIR 6000 SERIES RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. NO MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Laceration(s)
MAUDE report 18669487 ↗MalfunctionJan 18, 2024Insufficient Device Problem Information; Sharp Edges; Insufficient Device Problem Information; Sharp Edges
THE USER FACILITY REPORTED THAT THREE EMPLOYEES OBTAINED CUTS TO THEIR HANDS WHILE CLEANING THEIR RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. NO MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Laceration(s)
MAUDE report 18536742 ↗MalfunctionJan 3, 2024Insufficient Device Problem Information; Sharp Edges; Insufficient Device Problem Information; Sharp Edges
THE USER FACILITY REPORTED THAT AN EMPLOYEE OBTAINED AN INJURY (LACERATION) TO THEIR HAND WHILE CLEANING THEIR RELIANCE ENDOSCOPE DRYING AND STORAGE CABINET. IT IS UNKNOWN IF THE EMPLOYEE SOUGHT OR RECEIVED MEDICAL TREATMENT.
Patient problems: Laceration(s)
MAUDE report 18435133 ↗
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.
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