XIA IS2739XLP02Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327279344), received between Apr 6, 2016 and Oct 3, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 3, 2018Break; Fracture; Fracture

  K-WIRE FRACTURED DURING SURGERY. NO ADVERSE CONSEQUENCES WERE REPORTED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7931302 ↗
• MalfunctionApr 6, 2016Break

  IT WAS REPORTED THAT DURING THE SURGERY, THE SURGEON USED THE CANNULATED PROBE. THE VERTEBRAL BODY OF THE PATIENT BONE SCLEROSIS, SO THE SURGEON HIT THE PROBE WITH A HAMMER. WHEN THE SURGEON TRIED TO PULL OUT THE INTERNAL PROBE K-WIRE, BASE OF PROBE K-WIRE BROKE. THE SURGEON REMOVED THE BROKEN PROBE K-WIRE.

  Patient problems: No Code Available

  MAUDE report 5551957 ↗