TELIGEN 2860-01-120Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034548678), received between Oct 2, 2023 and Oct 2, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

Recent adverse event reports

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

• MalfunctionOct 2, 2023Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT ON (B)(6) 2023 DURING POSTERIOR SPINAL FUSION THE RIGID ARM THAT CONNECTS THE SCREW POST TO THE TELIGEN PORT, WAS NOT PROPERLY CONNECTING ONTO THE SCREW POST. SURGEON HAD TO FORCE THE RIGID ARM ONTO THE SCREW POST. SURGERY WAS COMPLETED SUCCESSFULLY WITH A SURGICAL DELAY OF THREE (3) MINUTES. THIS REPORT IS FOR ONE (1) TELIGEN LOCKING ARM. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17856289 ↗