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COUGAR 189160508Recalls & reported problems

Medos International Sàrl · COUGAR LS LATERAL CAGE SYSTEM LORDOTIC IMPLANT 18 x 8 x 60mm · Class 2 · Implant

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 10705034166162), received between Jul 17, 2019 and Jul 17, 2019 — 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

  • Foreign Body In Patient1
  • No Code Available1
  • Weakness1

Recent adverse event reports

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

  • InjuryJul 17, 2019Migration; Migration

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, PATIENT HAD L4-5 DIRECT LATERAL INTERBODY FUSION 7 DAYS PRIOR. THE PATIENT BEGAN HAVING LEG/HIP FLEXOR WEAKNESS AND CAME TO THE EMERGENCY ROOM. IT WAS DETERMINED THAT THE CAGE HAD MIGRATED. THERE WERE UNKNOWN PATIENT CONSEQUENCES. THE PATIENT REQUIRE REVISION SURGERY ON (B)(6) 2019 DUE TO CAGE MIGRATION. THIS COMPLAINT INVOLVES ONE (1) DEVICE.

    Patient problems: Foreign Body In Patient; No Code Available; Weakness

    MAUDE report 8798051 ↗

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Sources and updates

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