EXPEDIUM 175450010Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034251684), received between Apr 19, 2018 and Aug 8, 2018 — classified as 2 injuries.

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 16, 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.

• InjuryAug 8, 2018Loose or Intermittent Connection; Loose or Intermittent Connection

  DURING THE POST OP CONTROL THE SURGEON (DR (B)(6)) HAS SEEN ON XRAYS THAT ONE OF THE LOWER OFFSET CONNECTOR HAS MOVED AND WAS NO MORE IN THE ORIGINAL POSITION. THE X-RAY CAN BE FOUND ENCLOSED. ALSO A PICTURE INCLUDING ALL PRODUCT CODES AND LOT NUMBERS WHICH HAD BEEN USED CAN BE FOUND ENCLOSED. INITIAL PROCEDURE WAS ON (B)(6) 2018.

  Patient problems: Spinal Column Injury

  MAUDE report 7762563 ↗
• InjuryApr 19, 2018Migration or Expulsion of Device; Migration or Expulsion of Device

  DURING THE POST OP CONTROL THE SURGEON AND THE PATIENT HAVE SEEN ON XRAYS THAT ONE OF THE LOWER OFFSET CONNECTOR HAS MOVED AND WAS NO MORE IN THE ORIGINAL POSITION. THE PATIENT ALSO WROTE A COMPLAINT LETTER ON IT. THIS LETTER AND THE X-RAY CAN BE FOUND ENCLOSED. PROCEDURE: LUMBAR FIXATION + PLIF.

  Patient problems: Depression; Not Applicable; Spinal Column Injury

  MAUDE report 7442847 ↗