LCP 02.104.030Recalls & reported problems
Synthes GmbH · 3.5MM LCP EXTRA-ARTICLR DISTAL HUMERUS PL 10H/LT 230MM LONG · Class 2 · Implant
All models of LCP (367)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982029164), received between Jul 12, 2018 and Jul 12, 2018 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Pocket Erosion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 12, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT IMPLANTATION OF TWO (2) LOCKING COMPRESSION PLATE (LCP) DISTAL HUMERAL PLATES AND UNKNOWN SCREWS ON (B)(6) 2018. ON AN UNKNOWN DATE, PATIENT DEVELOPED HARDWARE ISSUES. ON (B)(6) 2018, PATIENT UNDERWENT HARDWARE REMOVAL DUE TO THE PLATES BREAKING THROUGH THE SKIN. THERE WAS NO SURGICAL DELAY REPORTED. PROCEDURE WAS COMPLETED SUCCESSFULLY AND PATIENT STATUS WAS STABLE. THIS IS REPORT 1 OF 3 FOR (B)(4).
Patient problems: Pocket Erosion
MAUDE report 7681391 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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