Medline DYND19140Recalls & reported problems
Medline Industries, Inc. · SET,IRRIGATION,CYSTO/TUR · 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 10884389942604), received between Sep 28, 2026 and Sep 28, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Disconnection” (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.
Reports received per month
Most reported problems
Device problems
- Disconnection1
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.
MalfunctionSep 28, 2026Disconnection
It was reported that the tubing is disconnecting from the stop cock very easily.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916831 ↗
Other System, irrigation, urological devices
- MED-RX 10-4001Canadian Hospital Specialties Limited · System, Irrigation, Urological1 recall0 reports
- Arthromatic/Uromatic 2C4041Baxter International Inc. · System, irrigation, urological40 reports
- MEDLINE DYND19122Medline Industries, Inc. · System, irrigation, urological7 reports
- MEDLINE DYND19124Medline Industries, Inc. · System, irrigation, urological4 reports
- MEDLINE DYND19120Medline Industries, Inc. · System, irrigation, urological3 reports
- Irrigation Set 313003B. Braun Medical Inc. · System, irrigation, urological2 reports
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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