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CONCORDE 187850208Recalls & reported problems

Medos International Sàrl · CONCORDE INLINE SPINAL SYSTEM LORDOTIC IMPLANT STRAIGHT 9 x 8 x 25mm, 5 DEGREES · Class 2 · Implant

All models of CONCORDE (24)

Data updated Oct 16, 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 10705034141558), received between Sep 12, 2018 and Sep 12, 2018 — classified as 1 malfunction.

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

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionSep 12, 2018Break; Break

    IT WAS REPORTED THAT DEVICE #(B)(4) JAMMED BETWEEN THE L5-S1 AND WHEN BEING REMOVED THROUGH ANTERIOR ACCESS THE IMPLANT BROKE INTO TWO PIECES. THIS WAS REPORTED TO SYNTHES VOICEMAIL AND ENTERED AS (B)(4))

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7870135 ↗

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Sources and updates

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