EXPEDIUM 179762120SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034270012), received between Aug 26, 2021 and Jan 5, 2024 — classified as 2 injuries.

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.

• InjuryJan 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN SWITZERLAND AS FOLLOWS: THIS REPORT IS BEING FILED AFTER THE REVIEW OF A CLINICAL EVALUATION REPORT (CER) FROM A DATABASE RELATED RESEARCH ACTIVITY (DRRA): SPINE TANGO SOA REPORT - TLIF. THE FOLLOWING COMPLICATIONS HAVE BEEN IDENTIFIED: NEUROCOMPRESSION. COMPLICATION TIME/INTERVENTION. REPEAT SURGERY. THIS IS FOR DEPUY SYNTHES SPINE EXPEDIUM SPINE SYSTEM ROD 5.5 X 120MM. THIS IS REPORT 2 OF 4 FOR (B)(4).

  Patient problems: Nerve Damage

  MAUDE report 18453658 ↗
• InjuryAug 26, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE PATIENT HAD SUFFERED FROM THE ADJACENT DISEASE. ON (B)(6) 2021 A REVISION SURGERY WAS PERFORMED WITHOUT FURTHER ISSUE. THE PRIMARY PROCEDURE WAS PERFORMED IN 2008 AND EXPEDIUM DI WAS APPLIED. THIS COMPLAINT INVOLVES TWENTY (20) DEVICES. THIS REPORT INVOLVES ONE (1) ROD, 120MM. THIS IS REPORT 19 OF 20 FOR (B)(4).

  Patient problems: Osteolysis

  MAUDE report 12374722 ↗