Reliance 6000 Series (REF REC6202DSA)Recalls & reported problems
Corporation Steris Canada · The 6000 Series Reliance Endoscope Drying and Storage Cabinet, 20 Scopes, Add-on (requires connectors) is designed to ensure a clean storage location for disinfected endoscopes and to protect the endoscopes from damage while in storage. · Class 2
All models of Reliance (8)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00724995179854), received between Jan 3, 2024 and Jul 31, 2026 — classified as 1 injury, 3 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Insufficient Device Problem Information4
- Sharp Edges3
Patient problems
- Laceration(s)4
Recent adverse event reports
The 4 most recent of 4 reports, 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 ↗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 ↗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 Endoscope maintenance system devices
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system5 reports
- RELIANCE Reliance 6500Steris Corporation · Endoscope maintenance system3 reports
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system2 reports
- ENDODRY Storage and Drying CabinetCantel Medical (Italy) Srl · Endoscope maintenance system2 reports
- RELIANCE Reliance 6500Steris Corporation · Endoscope maintenance system2 reports
- RELIANCE Reliance 6500 ConnectorsSteris Corporation · Endoscope maintenance system2 reports
- AMSCO Drying CabinetCorporation Steris Canada · Endoscope maintenance system2 reports
- Reliance 6000 SeriesCorporation Steris Canada · Endoscope maintenance system1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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