M.U.S.T. MINI Cross connector 03.75.715Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630040706674), received between Sep 4, 2019 and Sep 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Malposition of Device” (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

Recent adverse event reports

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

• MalfunctionSep 4, 2019Malposition of Device; Mechanics Altered

  STD CROSS CONNECTOR LENGTH 37MM: ALTHOUGH THE MEASURED VALUE OF ROD DISTANCE WAS 37MM, IT WAS NOT ABLE TO SET. STD CROSS CONNECTOR LENGTH 44MM: ALTHOUGH THERE WAS NO PROBLEM FOR THE SIZE OF STD CROSS CONNECTOR LENGTH 44MM, THE CONNECTION PART WITH ROD DID NOT MOVE SMOOTHLY. MOREOVER THE CONNECTION PART WITH ROD WAS THICK, SO IN ORDER TO USE IT THE SURGEON NEEDED TO REMOVE THE BONE ADDITIONALLY. THEREFORE THE SURGEON WAS NOT ABLE TO USE IT FOR THE SURGERY. THE SURGEON FINISHED THE SURGERY WITHOUT USING THE STD CROSS CONNECTOR. DUE TO THIS EVENT THE SURGERY WAS PROLONGED ABOUT 20 MINUTES. IT WAS HARD TO USE IT BECAUSE THE CONNECTION PART WITH ROD DID NOT MOVE SMOOTHLY AND IT WAS THICK. IT DID NOT MAKE SENSE TO USE IT IN CASE ADDITIONALLY BONE REMOVE IS REQUIRED.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8959261 ↗