T2 1806-1006Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04546540196552), received between Sep 29, 2015 and Sep 1, 2026 — classified as 1 injury, 5 malfunctions.

The most frequently reported specific device problem is “Break” (3 reports).

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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjurySep 1, 2026Fracture

  Patient problems: Foreign Body In Patient

  MAUDE report 50543812 ↗
• MalfunctionOct 8, 2020Positioning Failure; Failure to Align; Positioning Failure; Failure to Align

  FEMUR TARGET DEVICE 1806-1008/1806-1006, MISSDRILLING. STRIKE PLATE 1806-0150 COULD NOT BE SCREWED IN REPLACEMENT WAS AVAILABLE. SURGICAL DELAY OF 30MIN. NOT LONGER. NO OTHER CONSEQUENCES REPORTED. ADDITIONAL INFORMATION RECEIVED FROM THE OP LEAD: THE MISDRILLING OCCURRED AT THE PROXIMAL END THE ISSUE WAS RESOLVED BY USING SECOND TARGETING ARM AND LATER ORDERED NO PATIENT IMPACT, ONLY 30MIN OP TIME INCREASE THE THREADING OF STRIKE PLATE IMPACTED IN A WAY THAT IT CANNOT BE THREADED INTO THE TARGETING ARM ANYMORE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 10653188 ↗
• MalfunctionMar 27, 2020Material Fragmentation; Material Fragmentation

  IT WAS REPORTED, METAL ABRASION OCCURRED WHEN CONNECTING THE STRIKE PLATE AND THE NAIL HANDLE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9891025 ↗
• MalfunctionDec 19, 2018Break

  BROKEN IMPACTOR IN TARGETING DEVICE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8182769 ↗
• MalfunctionSep 29, 2015Break; Device Slipped

  IT WAS REPORTED THAT DURING A RETRO GRADE FEMORAL NAIL PROCEDURE, THE THREADS THAT HOLD THE IMPACTOR ON ARE STRIPPED ON BOTH OF THE T2 FEMORAL NAIL TRAYS - BOTH SLEEVES ARE STRIPPED AND DO NOT HOLD THE NAIL ANY LONGER. NO ADVERSE CONSEQUENCE TO PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 5110749 ↗
• MalfunctionSep 29, 2015Break; Device Slipped

  IT WAS REPORTED THAT DURING A RETRO GRADE FEMORAL NAIL PROCEDURE, THE THREADS THAT HOLD THE IMPACTOR ON ARE STRIPPED ON BOTH OF THE T2 FEMORAL NAIL TRAYS - BOTH SLEEVES ARE STRIPPED AND DO NOT HOLD THE NAIL ANY LONGER. NO ADVERSE CONSEQUENCE TO PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 5110736 ↗