Skip to content

M.U.S.T. MINI Rod 03.75.600Recalls & reported problems

Medacta International SA · Rod Ti ø3.5 x 80mm (sterile) · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630030864988), received between Jul 13, 2021 and Jul 13, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 18, 2026.

Most reported problems

Device problems

  • Loose or Intermittent Connection1
  • Unintended Movement1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryJul 13, 2021Loose or Intermittent Connection; Unintended Movement

    C3-C6 FIXATION, SURGERY PERFORMED ON JUNE 16. ON THE NEXT DAY THE SURGEON TOOK THE CT IMAGE AND CONFIRMED THE RODS DISENGAGEMENT FROM THE PEDICLE SCREWS. THE SURGEON CONFIRMED 2 SET SCREWS ON THE C4 COMPLETELY DISENGAGED AND REMAINED 6 SET SCREWS LOOSENED. NO CROSS CONNECTOR USED AT THE PRIMARY SURGERY. ALL IMPLANTS WERE REVISED. THE INSTRUMENTS USED DID NOT SHOW ANY PROBLEM DURING OTHER SURGERIES.

    Patient problems: Failure of Implant

    MAUDE report 12159037 ↗

Other Appliance, Fixation, Spinal Interlaminal devices

All Appliance, Fixation, Spinal Interlaminal devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page