DISTRACTION, INTERNAL 26-706-23-09Recalls & reported problems

KLS-Martin L.P. · DIST, FINGER, ZURICH 1, GENOS MINI, FRONT DRV, RIGHT, 2.0-2.3 MM SCREW, TI-6AL-4V · Class 2

All models of DISTRACTION, INTERNAL (67)

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 00888118054234), received between Oct 29, 2025 and Oct 29, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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.

Reports received per month

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

Most reported problems

Device problems

Fracture1

Patient problems

Insufficient Information1

Recent adverse event reports

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

InjuryOct 29, 2025Fracture; Fracture
IT WAS REPORTED THE DISTRACTOR FRACTURED DURING THE DISTRACTION PHASE. IT WAS REMOVED AND REPLACED.
Patient problems: Insufficient Information
MAUDE report 23412890 ↗

Device details

UDI-DI	`00888118054234`
Brand	DISTRACTION, INTERNAL
Model	26-706-23-09
Company	KLS-Martin L.P.
Product code	JEC · COMPONENT, TRACTION, INVASIVE
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Oct 19, 2023

Device type (GMDN): Orthopaedic surgical distractor, internal

A hand-held manual surgical instrument designed to invasively distract (force apart) two bone surfaces to enable a surgical procedure. It typically aids in fracture reduction by helping to temporarily stabilize bones prior to definitive surgical fixation. It typically consists of a central threaded spindle, a static endpiece and a sliding carriage that can be adjusted using spindle nuts to/from the endpiece to widen or shorten the gap; it facilitates the attachment of orthopaedic bone pins (Schanz screws) screwed into the bones to be distracted. It is typically used for multiple injuries when it is advantageous to perform procedures on a standard operating table. This is a reusable device.

Other COMPONENT, TRACTION, INVASIVE devices

HOFFMANN 4940-1-020
Stryker GmbH · COMPONENT, TRACTION, INVASIVE
1 recall1 report
NA 03.306.002
Synthes GmbH · COMPONENT, TRACTION, INVASIVE
5 reports
NA 03.306.003
Synthes GmbH · COMPONENT, TRACTION, INVASIVE
5 reports
NA 03.306.001
Synthes GmbH · COMPONENT, TRACTION, INVASIVE
4 reports
BREMER 3D HALO CROWN 292301001
Depuy Spine, LLC · COMPONENT, TRACTION, INVASIVE
2 reports
NA 03.306.000
Synthes GmbH · COMPONENT, TRACTION, INVASIVE
2 reports
Anjon Bremer Halo System Small Halo Crown Sterile
Anjon Holdings LLC · Component, Traction, Invasive
1 report
PIP Fix PFX-426
Hand Biomechanics Lab Inc · Component, Traction, Invasive
1 report

All COMPONENT, TRACTION, INVASIVE 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page