LCP 242.126SRecalls & reported problems
Synthes GmbH · 4.5MM LCP® PROXIMAL FEMUR HOOK PLATE 14 HOLES/349MM-STERILE · 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 10886982168191), received between May 16, 2019 and May 16, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Bone Fracture(s)1
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 16, 2019Break; Break
IT WAS REPORTED THAT ON (B)(6) 2019, THE PATIENT UNDERWENT PROXIMAL FEMUR REVISION DUE TO BROKEN PLATE. THE FEMUR AND PLATE BROKE WITHIN THE LAST FEW WEEKS. OPERATED ON TWO MONTHS AGO. THE PATIENT WAS COMPLIANT AN DID NOT WALK AS PER DOCTORS REQUEST OF CARE. THE SURGEON ORIGINALLY IMPLANTED PROXIMAL FEMUR HOOK PLATE ALONG WITH THE UNKNOWN CABLES AND UNKNOWN SCREWS TWO MONTHS AGO. THE PLATE BROKE BELOW THE STEM OF HIP THAT WAS IN THE PATIENT. THE BROKEN FRAGMENTS WERE REMOVED. THERE WAS NO FRAGMENTS GENERATED FROM THE BROKEN DEVICE. THERE WAS NO SURGICAL DELAY. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH NO SURGICAL DELAY. THE FEMUR WAS PROPERLY ALIGNED LATERALLY AND ON ANTEROPOSTERIOR. CONCOMITANT DEVICES: CABLES (PART#UNKNOWN, LOT#UNKNOWN, QUANTITY UNKNOWN), SCREWS (PART#UNKNOWN, LOT#UNKNOWN, QUANTITY UNKNOWN). THIS REPORT IS FOR ONE (1) 4.5MM LCP FEMUR PLATE. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Bone Fracture(s); No Code Available
MAUDE report 8616118 ↗
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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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