Illico 73600-050Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00844856043510), received between May 7, 2019 and May 7, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 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 7, 2019Fracture

  ON (B)(6) 2019 A PATIENT RETURNED TO THE SURGEON'S OFFICE COMPLAINING OF RECENT INCREASED PAIN. X-RAYS TAKEN THAT DAY REVEALED A FRACTURED ILLICO ROD. REVISION SURGERY WILL BE CONDUCTED BUT HAS NOT YET BEEN SCHEDULED. THE ILLICO POSTERIOR FIXATION SYSTEM WAS ORIGINALLY IMPLANTED ON (B)(6) 2018.

  Patient problems: Pain

  MAUDE report 8586783 ↗

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