LCS MILESTONE 2287-40-000Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS MILESTONE FEMORAL IM GUIDE SMALL STANDARD LARGE · Class 1
All models of LCS MILESTONE (14)
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 10603295110149), received between Sep 11, 2022 and Sep 11, 2022 — 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 18, 2026.
Most reported problems
Device problems
- Device-Device Incompatibility1
- Material Deformation1
- Mechanical Jam1
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.
MalfunctionSep 11, 2022Device-Device Incompatibility; Material Deformation; Mechanical Jam; Device-Device Incompatibility; Material Deformation; Mechanical Jam
IT WAS REPORTED THE SURGEON WAS UNABLE TO REMOVE THE CUTTING BLOCK FROM THE GUIDE. LEVER ON THE GUIDE SEIZED. ANOTHER DISTAL CUT BLOCK WAS USED TO COMPLETE THE CASE. SURGICAL DELAY OF 30 MINUTES OCCURRED. AFTER THE SURGERY, THE LEVER WAS STUCK BY HUMAN POWER AND COULD FINALLY BE REMOVED BY HITTING IT WITH A HAMMER. ACCORDING TO THE SALES REP, THE LOCKING ROD PART THAT IS CONNECTED TO THE LEVER APPEARS TO BE DEFORMED, AND IT IS POSSIBLE THAT IT MAY HAVE BEEN ENGAGED DURING THE FIXATION PROCESS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15397950 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 reports
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