Skip to content

EXPEDIUM 279763660Recalls & reported problems

Medos International Sàrl · EXPEDIUM SPINE SYSTEM SI LATERAL REDUCTION SLEEVE 6.35 370mm · Class 1

All models of EXPEDIUM (291)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034201054), received between Apr 12, 2021 and Apr 12, 2021 — classified as 1 malfunction.

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

Device problems

  • Material Deformation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionApr 12, 2021Material Deformation; Material Deformation

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING AND UNKNOWN PROCEDURE THE OUTER SLEEVE OF REDUCTION TOWER WAS BENT DURING ROD REDUCTION. SURGICAL DELAY IS UNKNOWN. THERE WERE NO PATIENT CONSEQUENCES. PROCEDURE OUTCOME IS UNKNOWN. CONCOMITANT DEVICE REPORTED: UNKNOWN ROD (PART# UNKNOWN, LOT# UNKNOWN, QUANTITY UNKNOWN). THIS COMPLAINT INVOLVES ONE (1) DEVICE. THIS REPORT IS 1 OF 1 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11648279 ↗

Other CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY devices

All CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page