Suction Valve MD-493 (REF N6177801)Recalls & reported problems
Olympus Medical Systems Corp. · Class 2
All models of SUCTION VALVE (5)
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 04953170438196), received between Jul 24, 2023 and Jul 24, 2023 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Device Reprocessing Problem” (5 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.
Most reported problems
Device problems
- Device Reprocessing Problem5
- Microbial Contamination of Device5
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.
MalfunctionJul 24, 2023Device Reprocessing Problem; Microbial Contamination of Device; Device Reprocessing Problem; Microbial Contamination of Device
THE FOLLOWING PATIENT IDENTIFIERS ARE RELATED TO THIS EVENT: (B)(6), MD-493: SUCTION VALVE -1; (B)(6), MD-493: SUCTION VALVE -2; (B)(6), MD-493: SUCTION VALVE -3; (B)(6), MD-493: SUCTION VALVE -4; (B)(6), MD-493: SUCTION VALVE -5; (B)(6), MD-493: SUCTION VALVE -6; (B)(6), MD-493: SUCTION VALVE -7; (B)(6), LF-TP, SN (B)(6); (B)(6), LF-GP, SN (B)(6); (B)(6), LF-GP, SN (B)(6); (B)(6), LF-TP, SN (B)(6); (B)(6), LF-GP, SN (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17386270 ↗MalfunctionJul 24, 2023Device Reprocessing Problem; Microbial Contamination of Device; Device Reprocessing Problem; Microbial Contamination of Device
THE FOLLOWING PATIENT IDENTIFIERS ARE RELATED TO THIS EVENT: (B)(6), MD-493: SUCTION VALVE -1. (B)(6), MD-493: SUCTION VALVE -2. (B)(6), MD-493: SUCTION VALVE -3. (B)(6), MD-493: SUCTION VALVE -4. (B)(6), MD-493: SUCTION VALVE -5. (B)(6), MD-493: SUCTION VALVE -6. (B)(6), MD-493: SUCTION VALVE -7. (B)(6), LF-TP, SN (B)(6). (B)(6), LF-GP, SN (B)(6). (B)(6), LF-GP, SN (B)(6). (B)(6), LF-TP, SN (B)(6). (B)(6), LF-GP, SN (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17386083 ↗MalfunctionJul 24, 2023Device Reprocessing Problem; Microbial Contamination of Device; Device Reprocessing Problem; Microbial Contamination of Device
THE FOLLOWING PATIENT IDENTIFIERS ARE RELATED TO THIS EVENT: (B)(6), MD-493: SUCTION VALVE -1 (B)(6), MD-493: SUCTION VALVE -2 (B)(6), MD-493: SUCTION VALVE -3 (B)(6), MD-493: SUCTION VALVE -4 (B)(6), MD-493: SUCTION VALVE -5 (B)(6), MD-493: SUCTION VALVE -6 (B)(6), MD-493: SUCTION VALVE -7 (B)(6), LF-TP, SN (B)(6). (B)(6), LF-GP, SN (B)(6). (B)(6), LF-GP, SN (B)(6). (B)(6), LF-TP, SN (B)(6). (B)(6), LF-GP, SN (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17386064 ↗MalfunctionJul 24, 2023Device Reprocessing Problem; Microbial Contamination of Device; Device Reprocessing Problem; Microbial Contamination of Device
RELATED PATIENT IDENTIFIERS: (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17385621 ↗MalfunctionJul 24, 2023Device Reprocessing Problem; Microbial Contamination of Device; Device Reprocessing Problem; Microbial Contamination of Device
THE FOLLOWING PATIENT IDENTIFIERS ARE RELATED TO THIS EVENT: (B)(6), MD-493: SUCTION VALVE -1. (B)(6), MD-493: SUCTION VALVE -2. (B)(6), MD-493: SUCTION VALVE -3. (B)(6), MD-493: SUCTION VALVE -4. (B)(6), MD-493: SUCTION VALVE -5. (B)(6), MD-493: SUCTION VALVE -6. (B)(6), MD-493: SUCTION VALVE -7. (B)(6), LF-TP, SN (B)(6). (B)(6), LF-GP, SN (B)(6). (B)(6), LF-GP, SN (B)(6). (B)(6), LF-TP, SN (B)(6). (B)(6), LF-GP, SN (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17379488 ↗
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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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