SYMPHONY 2020-00-405Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034532769), received between Jun 12, 2025 and Apr 15, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 15, 2026Material Integrity Problem

  IT WAS REPORTED DURING A SURGERY ON AN UNKNOWN DATE, THE SURGEON SAID THAT HE FELT SOMETHING STRANGE WHILE TIGHTENING THE NUT, BUT IT IS UNCLEAR WHEN IT BROKE. HOWEVER, THE FINAL TIGHTENING WAS MANAGED, SO IT DID NOT AFFECT THE PATIENT OR THE PROCEDURE. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH NO DELAY.NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24888642 ↗
• MalfunctionJun 12, 2025Material Deformation; Material Deformation

  IT WAS REPORTED THAT THIS WAS A POSTERIOR CERVICAL DISCECTOMY AND FUSION FOR OPLL. DURING SURGERY, IT WAS CONFIRMED THAT THE ROD THAT REMOVED THE SHAFT AT THE END OF THE NUT DRIVER WAS BENT. THE SURGEON ALSO FELT RESISTANCE WHEN INSERTING THE TROCAR, WHICH LED HIM TO BELIEVE THAT THE TIP OF THE MULTI POINT DRILL GUIDE MAY HAVE BEEN CRUSHED.THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22194824 ↗