EXPEDIUM 179771065Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034077611), received between Oct 10, 2017 and Oct 10, 2017 — classified as 1 injury.

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

• InjuryOct 10, 2017Device Slipped; Device Slipped

  IT WAS REPORTED THAT REVISION SURGERY WAS COMPLETED ON (B)(6) 2017. THE PATIENT WAS IMPLANTED WITH SYNTHES CLICK X AND PANGEA SCREWS AS WELL AS DEPUY SCREWS MORE THAN 5 YEARS AGO. THE ENTIRE CONSTRUCT IS FROM T-11 TO L-5. THE PATIENT WAS THEN IMPLANTED WITH MATRIX CONNECTORS AND RODS TO JOIN TOGETHER THE SYNTHES AND DEPUY SCREWS ON (B)(6) 2017. THE PATIENT WAS INVOLVED IN A CAR ACCIDENT ON AN UNKNOWN DATE AND PRESENTED WITH PAIN. HE FOLLOWED UP WITH THE SURGEON IN THE BEGINNING OF SEPTEMBER AND IT WAS DISCOVERED THAT THE RODS POPPED OUT OF THE CONNECTORS ON THE L-2 TO L-3. THE PATIENT WAS REVISED WITH A SYNTHES TRANSITIONAL ROD AND THE LOCKING CAPS WERE REPLACED.

  Patient problems: Failure of Implant; Injury; Pain

  MAUDE report 6937536 ↗