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pezo-T™ PEEK cage family CS 3315-07Recalls & reported problems

Ulrich GmbH & Co. KG · pezo-T, height 7 mm, length x width 29 x 11 mm, angle 5° · 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 04052536015955), received between Aug 3, 2017 and Aug 3, 2017 — classified as 1 injury.

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 18, 2026.

Most reported problems

Device problems

  • Break1
  • Use of Device Problem1

Patient problems

  • Failure of Implant1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • InjuryAug 3, 2017Break; Use of Device Problem; Break; Use of Device Problem

    CAGE BROKE WHILE SURGEON WAS TAPPING IT INTO PLACE, CAUSING A DELAY IN SURGERY. THE CAGE WAS REMOVED AND A NEW CAGE INSERTED WITH NO ISSUES.

    Patient problems: Failure of Implant; No Known Impact Or Consequence To Patient

    MAUDE report 6763948 ↗

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Sources and updates

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