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Kleiner KG2 system KG2 Static Lordotic 11x28x13x6°Recalls & reported problems

Baat Medical Products B.V. · KG2 Static Lordotic · Class 2 · Implant

Data updated Oct 18, 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 08720246782486), received between May 2, 2023 and May 2, 2023 — 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 18, 2026.

Most reported problems

Device problems

  • Migration1

Patient problems

  • Implant Pain1

Recent adverse event reports

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

  • InjuryMay 2, 2023Migration; Migration

    ON (B)(6) 2023, A CUSTOMER REPORTED AN EVENT THAT OCCURRED WITH A KLEINER KG2 CAGE. THEY HAD RECEIVED A MESSAGE FROM DR. (B)(6), A SURGEON, ON (B)(6) 2023 THAT A CAGE HAD PARTIALLY BACKED OUT AND THAT WOULD NEED A REVISION SURGERY. THE PATIENT AT SOME POINT (DATE UNKNOWN) AFTER THE INITIAL SURGERY COMPLAINED OF RECURRING PAIN. DR. (B)(6) TOOK THE PATIENT BACK TO THE OR AND ATTEMPTED TO FURTHER IMPACT THE CAGE INTO THE DISC SPACE. THE PATIENT SUBSEQUENTLY RETURNED AT SOME POINT AGAIN COMPLAINING OF RECURRING PAIN. A REVISION SURGERY IS PLANNED.

    Patient problems: Implant Pain

    MAUDE report 16851535 ↗

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Sources and updates

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