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LCP 426.662Recalls & reported problems

Synthes GmbH · 4.5MM TI CURVED BROAD LCP® PLATE 16 HOLES/300MM · 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 10886982217363), received between May 19, 2023 and May 19, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (1 report).

1 other recall cover devices cleared under the same FDA submission (K000682, K041911, K092609); they may or may not involve this specific model.

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

  • Failure of Implant1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 19, 2023Break; Break

    DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN GERMANY AS FOLLOWS: LEGAL CASE: IT WAS REPORTED FROM INBOX ON (B)(6) 2023 THAT A LETTER WAS RECEIVED FROM A LAW FIRM IN MUNICH. IT IS ABOUT ALLEGED PRODUCT LIABILITY DAMAGE. THE PATIENT WAS HOSPITALIZED ON (B)(6) 2022 IN THE ABOVE. A TITANIUM PLATE IS INSTALLED IN THE HOSPITAL FOR THE SUPPLY OF A FEMORAL NECK BOOK. THE METAL PLATE GOT BROKEN ON (B)(6) 2022 WITHOUT ANY RECOGNIZABLE INFLUENCE OF FORCE OR OTHER RECOGNIZABLE CAUSE. THE PATIENT SUSPECTS A MATERIAL DEFECT. THERE WAS A REVISION O. THE PATIENT SUFFERS FROM MULTIPLE SCLEROSIS. THIS REPORT IS FOR ONE (1) 4.5MM TI CURVED BROAD LCP® PLATE 16 HOLE THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

    Patient problems: Failure of Implant

    MAUDE report 16961800 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K000682, K041911, K092609. One submission often covers many models, so check the product and lot details in each record.

  • Z-0409-2014 · Jul 30, 2013 · Terminated
    Synthes 4.5 mm LCP Curved Condylar Plate Intended for buttressing multifragmentary distal femur fractures.

Other PLATE, FIXATION, BONE devices

All PLATE, FIXATION, BONE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page