Illico 73865-40Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00844856043190), received between Apr 1, 2020 and Apr 1, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Difficult to Remove” (1 report).

1 other recall cover devices cleared under the same FDA submission (K123623); they may or may not involve this specific model.

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.

• InjuryApr 1, 2020Difficult to Remove; Material Integrity Problem

  REVISION SURGERY WAS CONDUCTED (B)(6) 2020 TO EXTEND THE FIXATION FROM L4/5 TO L3-L5 DUE TO ADJACENT SEGMENT DISEASE. WHILE THE SURGEON TRIED TO REMOVE THE IMPLANTS, THE ID OF THE POLYAXIAL SCREW WAS STRIPPED/CRUSHED AND COULD NOT BE REMOVED. EVENTUALLY, AFTER A 2 HOUR DELAY AND ALTERNATIVE INSTRUMENTATION, THE SURGEON WAS ABLE TO REMOVE THE IMPLANTS. THE ILLICO MIS POSTERIOR FIXATION SYSTEM WAS ORIGINALLY IMPLANTED ON (B)(6) 2015 AT THE L4/5.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9910071 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K123623. One submission often covers many models, so check the product and lot details in each record.

• Z-2086-2013 · Jun 28, 2013 · Terminated
  Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico MIS Posterior Fixation System is intended to facilitate the surgical correction of noncervical spinal deformities by p