IDI 25217Recalls & reported problems
Tidi Products, LLC · IDI Urology Drain Bags Vinyl Sterile Fits Uroview 2600/2800 20 per Case · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00618125155682), received between Nov 11, 2019 and Nov 24, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Incorrect Measurement” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- No Apparent Adverse Event2
- Incorrect Measurement1
Patient problems
- No Known Impact Or Consequence To Patient2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 24, 2025Incorrect Measurement; Incorrect Measurement
REPORTING REJECTED PRODUCT DUE TO ADAPTERS NOT FITTING PROPERLY. TOO LOOSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23639391 ↗MalfunctionNov 11, 2019No Apparent Adverse Event; No Apparent Adverse Event
THE CUSTOMER'S END USER NOTIFIED THEM THAT THE DRAIN BAGS ARE LEAKING. THE LEAKAGE WAS NOTED AFTER THE ADAPTER WAS INSERTED INTO THE HOSE. THE LEAKAGE APPEARS TO HAVE OCCURRED BETWEEN THE ADAPTER AND HOSE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9305811 ↗MalfunctionNov 11, 2019No Apparent Adverse Event; No Apparent Adverse Event
THE CUSTOMER'S END USER NOTIFIED THEM THAT THE DRAIN BAGS ARE LEAKING. THE LEAKAGE WAS NOTED AFTER THE ADAPTER WAS INSERTED INTO THE HOSE. THE LEAKAGE APPEARS TO HAVE OCCURRED BETWEEN THE ADAPTER AND HOSE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9305810 ↗
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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