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EIT CIF cage CUI8090SRecalls & reported problems

EIT Emerging Implant Technologies GmbH · EIT CIF cage, H 9mm, 8°, S · Class 2 · Implant

Data updated Oct 13, 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 04260557770597), received between Mar 23, 2021 and Mar 23, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Device Slipped” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Slipped1

Patient problems

  • Failure of Implant1
  • Unspecified Tissue Injury1

Recent adverse event reports

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

  • InjuryMar 23, 2021Device Slipped; Device Slipped

    IT WAS REPORTED THAT THE PATIENTS HARDWARE BECOME LOOSE DUE TO POOR BONE QUALITY AND NON COMPLIANCE. PATIENT IS STATUS POST 3 LEVEL ANTERIOR CERVICAL DISCECTOMY AND FUSION (ACDF). INITIAL PROCEDURE WAS PERFORMED ON (B)(6) 2021. PATIENT HARDWARE WAS EXPLANTED ON (B)(6) 2021. PATIENT AND PROCEDURE OUTCOME WERE UNKNOWN. NO FURTHER INFORMATION PROVIDED. THIS REPORT IS FOR ONE (1) CIF UI H 9MM 8DEG S. THIS IS REPORT 5 OF 6 FOR (B)(4).

    Patient problems: Failure of Implant; Unspecified Tissue Injury

    MAUDE report 11558296 ↗

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Sources and updates

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