TELIGEN 2860-01-131Recalls & reported problems

Medos International Sàrl · TELIGEN TABLE MOUNT ADAPTER KNOB · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 10705034560519), 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

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 KNOB. THIS IS REPORT 1 OF 2 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17887018 ↗

Device details

UDI-DI	`10705034560519`
Brand	TELIGEN
Model	2860-01-131
Catalog no.	286001131
Company	Medos International Sàrl
Product code	JEB · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Aug 27, 2021

Device type (GMDN): Medical table clamp

A device that is designed to be used together with operating tables and certain kinds of examination/treatment tables. It can have different fixation/locking mechanisms, but is often designed to fit onto the side rails of such tables. It is used to hold different components and accessories onto the table providing added functionality. Such devices can be footrests, transducer holders, anaesthesia screen holders. The clamp allows for easy and safe adjustments of the position of these accessory devices and provides a secure locking mechanism. This is a reusable device.

Other TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL devices

TELIGEN 2860-01-132
Medos International Sàrl · TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL
1 report

All TABLE, SURGICAL WITH ORTHOPEDIC ACCESSORIES, MANUAL devices →

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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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