TELIGEN 2860-01-132Recalls & reported problems
Medos International Sàrl · TELIGEN Table Mount Adapter Fork · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034560502), received between Oct 6, 2023 and Oct 6, 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.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 6, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED ON AN UNKNOWN DATE, THAT BOTH THE TELIGEN TABLE MOUNT ADAPTOR KNOB AND TELIGEN TABLE MOUNT ADAPTOR FORK WERE NOT FUNCTIONING AS THEY SHOULD. THE KNOB IS UNABLE TO TIGHTEN DOWN AND EFFECTIVELY CAPTURE THE TELIGEN PORT HOLDER. THERE WERE NO PATIENT CONSEQUENCES REPORTED. THIS REPORT INVOLVES ONE TELIGEN TABLE MOUNT ADAPTER FORK. THIS IS REPORT 2 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17886088 ↗
Other TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL devices
- TELIGEN 2860-01-131Medos International Sàrl · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.