LCS MILESTONE 2287-54-000Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS MILESTONE FINISHING GDE .060 IN SLOTS STD+ · Class 1

Data updated Oct 18, 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 10603295110279), received between Nov 15, 2018 and Nov 15, 2018 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Twisted/Bent” (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.

Most reported problems

Device problems

Material Twisted/Bent1

Patient problems

No Code Available1

Recent adverse event reports

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

MalfunctionNov 15, 2018Material Twisted/Bent; Material Twisted/Bent
DURING PROCEDURE, WHEN THE FEMORAL FINISHING BLOCK WAS BEING POSITIONED ON THE RESECTED FEMORAL CONDYLES, THE BLOCK WAS FOUND TO NOT FIT ACCURATELY, ON CLOSER INSPECTION, THE BLOCK WAS FOUND TO BE "SPLAYED" SLIGHTLY. ALTERNATE STERILE RESECTION BLOCK SOURCED FROM ANOTHER SET. 5 MINUTE DELAY TO PROCEDURE. NO AE TO PATIENT.
Patient problems: No Code Available
MAUDE report 8075227 ↗

Device details

UDI-DI	`10603295110279`
Brand	LCS MILESTONE
Model	2287-54-000
Catalog no.	228754000
Company	Depuy Orthopaedics, Inc.
Product code	HWT · TEMPLATE
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	May 3, 2023

Device type (GMDN): Orthopaedic prosthesis implantation positioning instrument, reusable

A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use.

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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.

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