HOFFMANN 4933-2-180Recalls & reported problems

Stryker GmbH · Full Ring LRF · Class 2

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 07613252610625), received between Jan 28, 2025 and Jan 28, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

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

Most reported problems

Device problems

Break1
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.

InjuryJan 28, 2025Break; Fracture; Break; Fracture
AS REPORTED: RING BROKE ON HLRF FRAME IN PATIENT HOME. THE PATIENT NOTICED A NOISE ON CHRISTMAS EVE AND THEN ATTENDED CLINIC ON NEW YEAR'S EVE FOR REVIEW. DECISION REMAINS OUTSTANDING AS TO WHETHER OR NOT PATIENT WILL BE REVISED (ADVERSE CONSEQUENCES).
Patient problems: Insufficient Information
MAUDE report 21260502 ↗

Device details

UDI-DI	`07613252610625`
Brand	HOFFMANN
Model	4933-2-180
Company	Stryker GmbH
Product code	KTT · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
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	Jun 24, 2026

Device type (GMDN): External orthopaedic fixation system noninvasive component, single-use

A noninvasive, non-powered structural component of an external orthopaedic fixation system intended for bone/joint treatment (typically fracture stabilization, deformity correction, or distraction), in conjunction with an invasive bone pin (not included). It is in the form of a full or partial ring, rod (e.g., straight, curved, telescopic), plate, or connector (e.g., screw, bolt, nut, hinge, coupling, fastener); it is not a surgical instrument. This is a single-use device.

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices

PRECICE® Plating System LP4.5-DLF31
Nuvasive Specialized Orthopedics, Inc. · Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
3 recalls0 reports
R3 71364451
Smith & Nephew, Inc. · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
145 reports
DFS HA BONE SCREWS HAA60-15040
Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
2 recalls0 reports
DFS HA BONE SCREWS HAA60-15050
Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
2 recalls0 reports
DFS HA BONE SCREWS HAB60-12040
Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
2 recalls0 reports
DFS HA BONE SCREWS HAA60-13040
Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
2 recalls0 reports
DFS HA BONE SCREWS HAA60-18030
Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
2 recalls0 reports
DFS HA BONE SCREWS HAA60-15030
Biomet Orthopedics, LLC · APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT
2 recalls0 reports

All APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.