Illico 73600-045Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00844856043503), received between Feb 23, 2016 and Feb 23, 2016 — classified as 1 injury.

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

• InjuryFeb 23, 2016Break

  ABOUT THE THREE MONTHS AFTER THE SURGERY, THE REOPERATION [SIC] WAS PERFORMED BECAUSE CONFIRMED [SIC] THAT THE DISK SPACE OF THE PATIENT HAD BEEN PRESSED. DOCTOR RETRIEVED OUT [SIC] ALL IMPLANTED SCREWS AND RODS FROM THE PATIENT. THEN HE FOUND OUT THAT THE ROD WHICH HAD BEEN IMPLANTED ON THE RIGHT SIDE WAS BROKEN. AT THE CURRENT MOMENT, NO HEALTH INJURY OF THE PATIENT WAS CONFIRMED BY THIS INCIDENT.

  Patient problems: No Code Available

  MAUDE report 5455016 ↗

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