EIT LLIF cage LUI71460Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04260557836118), received between Mar 25, 2025 and Jul 3, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Migration” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJul 3, 2025Migration; Migration

  STUDY NO: (B)(6). CLINICAL ADVERSE EVENT RECEIVED FOR SURGICAL INTERVENTION - GRAFT SUBSIDENCE. DEVICE AND PROCEDURE (RELATEDNESS) . DEVICE RELATED: POSSIBLE. PROCEDURE RELATED: NOT RELATED. PROCEDURE: MIS. DATE OF EVENT: 07 NOV 2024. DATE OF IMPLANT: (B)(6) 2024. DATE OF REVISION: (B)(6) 2024. DEVICE LOCATION: L2-L3. TREATMENT/IMPACT: REQUIRED IN-PATIENT HOSPITALIZATION OR PROLONGATION OF EXISTING HOSPITALIZATION, SURGICAL INTERVENTION FOR THE STUDY SPINE SEGMENT.

  Patient problems: Insufficient Information

  MAUDE report 22393574 ↗
• InjuryMar 25, 2025Migration; Migration

  ADDITIONAL INFORMATION RECEIVED: EVENT DETAILS EVENT DATE: UN OCT 2024, ALERT DATE: 13 JUN 2025. EVENT OCCURRED COUNTRY OF EVENT: UNITED STATES, PROCEDURE: MIS, DATE OF PROCEDURE: (B)(6) 2024, LEVELS TREATED: L2-L3:YES,L3-L4:NO,L4-L5:NO,L5-S1:NO, EVENT DESCRIPTION: GRAFT SUBSIDENCE. ADDITIONAL EVENT DETAILS ADVERSE EVENT TERM: GRAFT SUBSIDENCE IS THIS A WORSENING OF AN EXISTING EVENT?: NO SITE AWARENESS DATE: 29 OCT 2024 START DATE: UN OCT 2024 TYPE OF EVENT: LOCAL/OPERATIVE SITE, SEVERITY: MODERATE, IS THE ADVERSE EVENT SERIOUS? : NO, RELATIONSHIP TO STUDY DEVICE: POSSIBLE, RELATIONSHIP TO PRIMARY STUDY PROCEDURE: NOT RELATED, OUTCOME: RECOVERED/RESOLVED, END DATE: (B)(6) 2025. DID THIS EVENT RESULT IN THE SUBJECT'S DISCONTINUATION OF THE STUDY? IF YES, COMPLETE THE STUDY DISCONTINUATION FORM.: NO INTERVENTION/TREATMENT (MARK 'NONE/OBSERVATION' OR ALL THAT APPLY.) NONE/OBSERVATION: NO DIAGNOSTIC INTERVENTION: YES SPECIFY: FLUORO MYELOGRAM SPINAL CANAL W/LP ON (B)(6) 2024 REHABILITATION (E.G. PT/OT): NO INJECTED MEDICATION: YES SPECIFY: PER NOTE: CHRONIC PAIN PROVIDER GAVE HIM SOME TRIGGER POINT INJECTIONS WHICH HELPED SOME. ASPIRATION: NO ORAL/TOPICAL MEDICATION: NO OTHER NON-SURG

  Patient problems: Insufficient Information; Pain

  MAUDE report 21686232 ↗