Medline DYND17407LRecalls & reported problems
Medline Industries, Inc. · METER,URINE,EXACT MEASURE,200ML,LF,LL · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277136946), received between Sep 8, 2026 and Sep 18, 2026 — classified as 2 malfunctions.
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
- Fitting Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 18, 2026Fitting Problem
It was reported that Patient arrived via transport from PACU with foley completely disconnected from urine collection bag. Per the reporter this event was a product issue, the size urethral foley (6 french) that was being used did not properly fit the collection bag (Urine Meter w/ Drain, item #2032, AKA (b)(6)).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50817950 ↗MalfunctionSep 8, 2026Disconnection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676376 ↗
Other DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE devices
- Dover P4P16XTSDCardinal Health 200, LLC · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE77 reports
- Dover P4P16TSDCardinal Health 200, LLC · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE61 reports
- Dover P4P16TSCardinal Health, Inc. · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE10 reports
- Dover P4P16XTSCardinal Health, Inc. · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE10 reports
- Dover P4P16SDCardinal Health 200, LLC · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE9 reports
- Dover P4P18TSCardinal Health, Inc. · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE2 reports
- Medline DYND27403Medline Industries, Inc. · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE1 report
- Medline DYND27403SMedline Industries, Inc. · DEVICE, URINE FLOW RATE MEASURING, NON-ELECTRICAL, DISPOSABLE1 report
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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