Illico 73734Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00844856041721), received between Jan 3, 2019 and Jan 3, 2019 — classified as 1 injury.

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

• InjuryJan 3, 2019Break; Patient-Device Incompatibility

  DURING A DIFFICULT MULTI-LEVEL SPONDY REDUCTION, TWO TOWERS BROKE WHILE UNDER REDUCTIONS AND TWO MORE BROKE DURING REMOVAL/DETACHMENT FROM THE SCREW. THE PATIENT WAS REPORTED TO HAVE USUALLY HARD DENSE BONE WHICH FORCED THE SURGEON TO DRILL 6 OF 8 PEDICLES. DURING REDUCTION, THE STRAIN ON THE INSTRUMENTS POPPING & CRACKING COULD BE HEARD. THE EVENT CAUSED A TWO HOUR DELAY IN THE CASE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8212517 ↗