WATER CONTAINER MAJ-902Recalls & reported problems
Olympus Medical Systems Corp. · "MAJ-902 C02 GAS/WATER CONTAIN CV-160/140" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 04953170022937), received between Oct 1, 2021 and Sep 6, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Contamination” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Contamination2
- Device Reprocessing Problem2
- Corroded1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 6, 2024Device Reprocessing Problem; Device Reprocessing Problem
IT WAS REPORTED THE WATER CONTAINER WAS WASHED WITH WATER, AND THEN WASHED WITH DETERGENT AND DISINFECTED OR STERILIZED AT THE END OF EACH DAY. THE ISSUE OCCURRED DURING REPROCESSING. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20159177 ↗MalfunctionFeb 22, 2024Device Reprocessing Problem; Device Reprocessing Problem
IT WAS REPORTED, THE WATER CONTAINER CLEANING CAP MAY HAVE BEEN REPROCESSED WITHOUT ATTACHING THE CAP TO THE MOUNTING RING DURING THE REPROCESSING. THERE WERE NO REPORTS OF PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18759777 ↗MalfunctionMay 9, 2022Contamination; Contamination
THE CUSTOMER CONTACTED OLYMPUS TO REPORT TWO OF THEIR MAJ-902 WATER BOTTLES HAVE SIGNS OF RUST ON THE INSIDE. THEY HAVE MANY MORE OF THESE BOTTLES AND HAVE NOT HAD THIS ISSUE BEFORE. THEY FOUND THE ISSUE DURING PREPARATION FOR USE IN AN UNSPECIFIED PROCEDURE, AND COMPLETED THE PROCEDURE WITH A SIMILAR DEVICE. THERE WAS NO REPORT OF PATIENT HARM. THIS EVENT IS RELATED TO PATIENT IDENTIFIER (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14340751 ↗MalfunctionMay 9, 2022Contamination; Contamination
THE CUSTOMER CONTACTED OLYMPUS TO REPORT TWO OF THEIR MAJ-902 WATER BOTTLES HAVE SIGNS OF RUST ON THE INSIDE. THEY HAVE MANY MORE OF THESE BOTTLES AND HAVE NOT HAD THIS ISSUE BEFORE. THEY FOUND THE ISSUE DURING PREPARATION FOR USE IN AN UNSPECIFIED PROCEDURE, AND COMPLETED THE PROCEDURE WITH A SIMILAR DEVICE. THERE WAS NO REPORT OF PATIENT HARM. THIS EVENT IS RELATED TO PATIENT IDENTIFIER (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14340608 ↗MalfunctionOct 1, 2021Corroded; Corroded
OLYMPUS MEDICAL SYSTEMS CORP. (OMSC) WAS INFORMED FROM THE USER THAT DURING PREPARATION FOR UNSPECIFIED PROCEDURE USING THE SUBJECT DEVICE IN COMBINATION WITH THE VIDEO PROCESSOR CV-290 (PATIENT WAS NOT UNDER ANESTHESIA), IT WAS FOUND THAT THERE WAS RUST AROUND THE GAS TUBE CONNECTOR OF THE LID OF THE SUBJECT DEVICE. THE USER REPLACED THE SUBJECT DEVICE TO ANOTHER SIMILAR DEVICE TO COMPLETE THE INTENDED PROCEDURE. THERE WAS NO REPORT OF PATIENT INJURY ASSOCIATED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12561609 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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