NA 109-015-1032Recalls & reported problems
Biedermann Motech GmbH & Co. KG · TELIX K Ti Cage 10x32mm 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 04250869607711), received between Sep 23, 2021 and Sep 23, 2021 — 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
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 23, 2021Migration; Migration
IT WAS REPORTED ON (B)(6) 2021 THAT THE SURGERY WAS PERFORMED TO REVISE AND REMOVE A MIGRATED TELIX K CAGE. THE GRAFT MIGRATED AND BACKED OUT IN THE CRITICAL ZONE NEAR SPINAL NERVED IN WHICH CAUSED PAIN IN PATIENT. THERE WERE NO REPORTS OF PATIENT IMPACT AS A RESULT OF THIS REVISION SURGERY. PRODUCT WILL NOT BE RETURNED.
Patient problems: Pain
MAUDE report 12521389 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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