XIA PRECISION SYSYEM IS3013XLPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327279474), received between May 2, 2018 and May 2, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Bent” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 2, 2018Fracture; Bent; Break; Fracture

  IT WAS REPORTED THAT WHILE ACCESSING PEDICLE WITH THE SPECIALTY CANNULATED PROBE WITH TROCAR, SURGEON WAS USING MALLET TO ADVANCE PROBE WITH TROCAR INSERTED, WHEN THE TIP OF THE PROBE BENT, CAUSING TROCAR TO BE PINCHED. WHEN ATTEMPTING TO REMOVE INNER TROCAR TO INSERT K WIRE, INNER TROCAR BROKE. THERE ARE NO REPORTS OF ADVERSE CONSEQUENCES TO THE PATIENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7480239 ↗