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EXPEDIUM 175450020Recalls & reported problems

Medos International Sàrl · EXPEDIUM SPINE SYSTEM SLOTTED CONNECTOR, EXTENDED 5.5/6.35mm · Class 2 · Implant

All models of EXPEDIUM (291)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034251707), received between Aug 31, 2018 and Aug 31, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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

Device problems

  • Migration1

Patient problems

  • Spinal Column Injury1

Recent adverse event reports

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

  • InjuryAug 31, 2018Migration; Migration

    IT WAS REPORTED THAT DR (B)(6) INFORMED US OF ANOTHER CONNECTOR WHICH HAD MOVED POST-OPERATIVELY. ON (B)(6) 2018: INITIAL PROCEDURE (OVERVIEW OF USED PRODUCT CAN BE FOUND IN THE ATTACHMENTS). ON (B)(6) 2018 A CT WAS TAKEN (POST-OP), BECAUSE OF SUDDEN OUTAGE OF THE LEFT LEG. THE CONNECTOR WAS STILL WELL POSITIONED. ON (B)(6) 2008 A RX WAS TAKEN AND IT BECAME CLEAR THAT THE CONNECTOR HAD MOVED (CT AND RX CAN BE FOUND IN TH ATTACHMENTS). REVISION TOOK PLACE ON (B)(6) 2008. DEFECTIVE IMPLANTS WILL BE RETURNED FOR ANALYSIS.

    Patient problems: Spinal Column Injury

    MAUDE report 7836717 ↗

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Sources and updates

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