LCS MILESTONE 2287-33-000Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS MILESTONE A/P RESECTION GUIDE STD · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 2
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295110088), received between Nov 1, 2018 and Jun 1, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (2 reports).

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

Device-Device Incompatibility2

Patient problems

Insufficient Information1
Not Applicable1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

MalfunctionJun 1, 2021Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE PIN GOT STUCK IN THE POSTERIOR REFERENCING HOLES ON THE STD AP BLOC. 5 MINUTES DELAY IN SURGERY WAS REPORTED.
Patient problems: Insufficient Information
MAUDE report 11916247 ↗
MalfunctionNov 1, 2018Device-Device Incompatibility; Device-Device Incompatibility
UPON USING THE RESECTION BLOCK AND ROD, THE SURGEON FOUND THAT THE ROD DIDN'T FIT THROUGH THE RESECTION BLOCK PROPERLY.
Patient problems: Not Applicable
MAUDE report 8029560 ↗

Device details

UDI-DI	`10603295110088`
Brand	LCS MILESTONE
Model	2287-33-000
Catalog no.	228733000
Company	Depuy Orthopaedics, Inc.
Product code	HTZ · INSTRUMENT, CUTTING, ORTHOPEDIC
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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