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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 1 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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

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