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DEPUY 2055-24-000Recalls & reported problems

Depuy (Ireland) · DEPUY FEMORAL HEAD SIZER 57/61mm · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
8
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295084556), received between Sep 11, 2018 and May 18, 2023 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Naturally Worn” (5 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 18, 2026.

Most reported problems

Device problems

  • Naturally Worn5
  • Scratched Material2
  • Illegible Information1
  • Insufficient Device Problem Information1

Patient problems

  • No Clinical Signs, Symptoms or Conditions4
  • No Consequences Or Impact To Patient4

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 18, 2023Scratched Material; Scratched Material

    IT WAS REPORTED THAT HEAD SIZERS PITTED NEED TO BE REPLACED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16952294 ↗
  • MalfunctionMay 18, 2023Scratched Material; Scratched Material

    IT WAS REPORTED THAT HEAD SIZERS PITTED NEED TO BE REPLACED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16952209 ↗
  • MalfunctionApr 18, 2022Naturally Worn; Illegible Information; Naturally Worn; Illegible Information

    IT WAS REPORTED THAT THE SIZERS FOR THE FEMORAL HEADS ARE FADED AND YOU CANNOT READ THEM. INSTRUMENTS ABOUT 10 YEARS OLD. WEAR AND TEAR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14137724 ↗
  • MalfunctionNov 4, 2021Naturally Worn; Naturally Worn

    IT WAS REPORTED THAT THE WRITING HAS FADED OFF. NO SURGICAL DELAY REPORTED. NO FURTHER INFORMATION RECEIVED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12751780 ↗
  • MalfunctionSep 11, 2018Naturally Worn; Naturally Worn

    MDR STAFF HAS INDICATED THAT PRODUCT IS WORN AND DAMAGED. PRODUCT IS NO LONGER FUNCTIONAL AND A REPLACEMENT IS REQUIRED. NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7864793 ↗
  • MalfunctionSep 11, 2018Naturally Worn; Naturally Worn

    MDR STAFF HAS INDICATED THAT PRODUCT IS WORN AND DAMAGED. PRODUCT IS NO LONGER FUNCTIONAL AND A REPLACEMENT IS REQUIRED. NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7864783 ↗
  • MalfunctionSep 11, 2018Naturally Worn; Naturally Worn

    MDR STAFF HAS INDICATED THAT PRODUCT IS WORN AND DAMAGED. PRODUCT IS NO LONGER FUNCTIONAL AND A REPLACEMENT IS REQUIRED. NO FURTHER INFORMATION IS AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7864781 ↗
  • MalfunctionSep 11, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    MDR STAFF HAS INDICATED THAT PRODUCT IS WORN AND DAMAGED. PRODUCT IS NO LONGER FUNCTIONAL.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7864778 ↗

Other TEMPLATE devices

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Sources and updates

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