LCS 2178-30-121Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS HIGH PERFORMANCE INSTRUMENTS RP TRIAL POST · Class 1
All models of LCS (45)
Data updated Oct 16, 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 10603295093992), received between Feb 5, 2019 and May 5, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 5, 2021Break; Break
IT WAS REPORTED THAT WHILE TRIALING, THE DOCTOR CONTINUED TO HIT THE POLY TRIAL REGARDLESS OF THE FACT THAT THE POST SITS PROUD AND PROMINENT OF THE TIBIAL BASE PLATE. BECAUSE OF THIS, THE TRIAL POST SNAPPED IN HALF. SURGERY WAS NOT DELAYED. TWO PIECES WERE RETRIEVED AND WILL BE RETURNING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11777702 ↗MalfunctionFeb 5, 2019Break; Break
IT WAS REPORTED THE HP RP TRIAL POST WAS BROKEN DURING A PROCEDURE ON (B)(6) 2019. THERE WERE NO FRAGMENTS GENERATED. THERE WAS NO SURGICAL DELAY AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO PATIENT CONSEQUENCE OR MEDICAL INTERVENTION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8304166 ↗
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
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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