UROLIFT IPN929371Recalls & reported problems
Teleflex Incorporated · UroLift 2 Implant Cartridge Handle Kit · Class 2 · Implant
All models of UROLIFT (13)
Data updated Oct 18, 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 10814932021470), received between Jul 10, 2026 and Sep 16, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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
- Adverse Event Without Identified Device or Use Problem1
- Detachment of Device or Device Component1
- Difficult to Remove1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 16, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Insufficient Information
MAUDE report 50786576 ↗MalfunctionSep 8, 2026Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50674140 ↗MalfunctionJul 10, 2026Difficult to Remove
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25780149 ↗
Other Implantable transprostatic tissue retractor system devices
- UroLift UL400-4Neotract, Inc. · Implantable Transprostatic Tissue Retractor System1 recall9 deaths144 reports
- UroLift UL400-4Neotract, Inc. · Implantable Transprostatic Tissue Retractor System1 recall3 reports
- UROLIFT IPN924184Teleflex Incorporated · Implantable transprostatic tissue retractor system1 death32 reports
- UROLIFT IPN918876Teleflex Incorporated · Implantable transprostatic tissue retractor system18 reports
- UROLIFT IPN923352Teleflex Incorporated · Implantable transprostatic tissue retractor system15 reports
- UROLIFT IPN055826Teleflex Incorporated · Implantable transprostatic tissue retractor system15 reports
- UROLIFT IPN056134Teleflex Incorporated · Implantable transprostatic tissue retractor system1 death10 reports
- UROLIFT IPN056885Teleflex Incorporated · Implantable transprostatic tissue retractor system10 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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