MPS Water Hose Kit 5303030Recalls & reported problems
Quest Medical Inc · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20634624530335), received between Jul 29, 2022 and Jul 29, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Connection Problem” (1 report).
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.
Most reported problems
Device problems
- Connection Problem1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 29, 2022Use of Device Problem; Connection Problem; Use of Device Problem
IT WAS REPORTED TO QUEST MEDICAL OF AN ALLEGED ISSUE WITH WATER HOSE CONNECTOR 5303030. PER THE REPORT, AFTER THE INDUCTION DOSE, THE WATER LINE HOSE CONNECTOR DISCONNECTED, SPRAYING WATER INTO THE STERILE FIELD. INSTRUMENTS HAD TO BE CHANGED OUT AND THE PATIENT WAS PUT ON ADDITIONAL ANTIBIOTICS. NO PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15136073 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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