LCS MILESTONE 2287-34-000Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS MILESTONE A/P RESECTION GUIDE STD+ · Class 1
All models of LCS MILESTONE (14)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295110095), received between Sep 27, 2017 and Sep 15, 2020 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (4 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
- Material Deformation4
- Device-Device Incompatibility3
- Naturally Worn3
- Mechanical Jam2
- Connection Problem1
- Difficult to Remove1
Patient problems
- Not Applicable4
- No Code Available1
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2020Mechanical Jam; Mechanical Jam
IT WAS REPORTED THAT THE FIXATION PIN SEIZED IN STD+ ANTERIOR/POSTERIOR CUTTING BLOCK. NO SURGICAL DELAY.
Patient problems: No Code Available; No Consequences Or Impact To Patient
MAUDE report 10538140 ↗MalfunctionApr 16, 2019Difficult to Remove; Connection Problem; Device-Device Incompatibility; Material Deformation; Naturally Worn; Difficult to Remove; Connection Problem; Device-Device Incompatibility; Material Deformation; Naturally Worn
ONCE THE INSTRUMENTS WERE OPENED THE NURSE WAS ASKED TO CHECK TO MAKE SURE THE DRILL AND ROD FIT THROUGH THE CENTRAL HOLE, IT WAS FOUND THAT IT DID NOT FIT THROUGH THE STD + A/P RESECTION BLOCK BUT DID FIT THROUGH THE OTHER SIZES.
Patient problems: Not Applicable
MAUDE report 8518730 ↗MalfunctionApr 15, 2019Device-Device Incompatibility; Material Deformation; Naturally Worn; Device-Device Incompatibility; Material Deformation; Naturally Worn
WHILE USING THE LCS MILESTONE INSTRUMENTS DURING A TOTAL KNEE REPLACEMENT, THE 9MM DRILL AND ROD DID NOT FIT THROUGH THE CENTRAL (IM HOLE) OF THE STD + A/P RESECTION BLOCK. THE OTHER SIZE BLOCKS WERE TRIED WITH THE DRILL AND ROD PASSING THROUGH AS INTENDED. A NEW SET WAS OPENED AND USED.
Patient problems: Not Applicable
MAUDE report 8514195 ↗MalfunctionApr 15, 2019Device-Device Incompatibility; Material Deformation; Naturally Worn; Device-Device Incompatibility; Material Deformation; Naturally Worn
WHILE USING THE LCS MILESTONE INSTRUMENTS DURING A TOTAL KNEE REPLACEMENT, THE 9MM DRILL AND ROD DID NOT FIT THROUGH THE CENTRAL (IM HOLE) OF THE STD + A/P RESECTION BLOCK. THE OTHER SIZE BLOCKS WERE TRIED WITH THE DRILL AND ROD PASSING THROUGH AS INTENDED. A NEW SET WAS OPENED AND USED.
Patient problems: Not Applicable
MAUDE report 8514188 ↗MalfunctionNov 29, 2018Mechanical Jam; Mechanical Jam
DURING OPERATION THE FEMORAL CANAL WAS DRILLED AS PER SURGICAL TECHNIQUE. THE DROP BECAME STUCK IN THE CENTRAL HOLE OF THE BLOCK AND JAMMED.
Patient problems: Not Applicable
MAUDE report 8115689 ↗MalfunctionSep 27, 2017Material Deformation; Material Deformation
IT WAS REPORTED THAT THE LCS MILESTONE STD + A/P BLOCK MIDDLE PIN HOLE ON THE POSTERIOR LEFT CLUSTER IS BURRED UP AND A PIN WILL NOT GO THROUGH IT.
Patient problems: No Information
MAUDE report 6898352 ↗
Other INSTRUMENT, CUTTING, ORTHOPEDIC devices
- SIGMA LCS 9505-01-230Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC95 reports
- ATTUNE 2544-00-522Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC58 reports
- SIGMA LCS 9505-01-229Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC56 reports
- SIGMA 2024-40-100Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC43 reports
- ATTUNE 2545-00-158Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC41 reports
- ATTUNE 2545-00-156Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC41 reports
- SIGMA 2024-40-200Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC40 reports
- ATTUNE 2545-00-155Depuy (Ireland) · INSTRUMENT, CUTTING, ORTHOPEDIC39 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.
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