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DHS 281.504Recalls & reported problems

Synthes GmbH · 130 DEG DHS® PLATE-SHORT BARREL 4 HOLES/78MM · Class 2 · Implant

Data updated Oct 13, 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 10886982177483), received between Nov 30, 2021 and Nov 30, 2021 — 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1

Recent adverse event reports

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

  • InjuryNov 30, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT ON (B)(6) 2021, PATIENT UNDERWENT A REMOVAL OF HARDWARE AND REVISION OF OPEN REDUCTION INTERNAL FIXATION(ORIF) LEFT FEMUR DUE TO FAILED FIXATION. LEFT HIP, FAILED DHS CONSTRUCT FOR SUBTROCH PROXIMAL FEMUR FRACTURE. THE ORIGINAL SURGERY WAS ON (B)(6) 2021. THIS REPORT IS FOR ONE (1) 130 DEG DHS PL-SHORT BARREL 4 HOLES/78. THIS IS REPORT 1 OF 7 FOR (B)(4).

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 12902352 ↗

Other DEVICE, FIXATION, PROXIMAL FEMORAL, IMPLANT devices

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Sources and updates

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