SELF CENTERING 2055-40-000Recalls & reported problems

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10603295084570), received between Nov 6, 2018 and Sep 10, 2026 — classified as 10 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 16, 2026.

Most reported problems

Recent adverse event reports

The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 10, 2026Break

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50721372 ↗
• MalfunctionOct 14, 2024Device-Device Incompatibility; Illegible Information; Device-Device Incompatibility; Illegible Information

  IT WAS REPORTED THAT HEAD TRIALS DID NOT FIT ON TRIAL STICK AND SIZES ARE NOT VISIBLE. THESE WERE FOUND AFTER THE CASE SO THERE WERE NO ADVERSE CONSEQUENCES AND THE PATIENT WAS NOT AFFECTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20439792 ↗
• MalfunctionOct 14, 2024Device-Device Incompatibility; Illegible Information; Device-Device Incompatibility; Illegible Information

  IT WAS REPORTED THAT THE HEAD TRIALS DID NOT FIT ONTO TRIAL STICK. THE SIZES ARE NOT VISIBLE ON THE HEAD TRIALS. THESE WERE FOUND AFTER THE CASE SO THERE WERE NO ADVERSE CONSEQUENCES AND THE PATIENT WAS NOT AFFECTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20439089 ↗
• MalfunctionOct 24, 2022Break; Break

  IT WAS REPORTED THAT TWO ITEMS BROKE DURING THE HEMI HIP ARTHROPLASTY. THE REPLACEMENTS WAS AVAILABLE, SO SURGERY WAS NOT DELAYED BECAUSE OF THIS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15657473 ↗
• MalfunctionMay 7, 2022Naturally Worn; Illegible Information; Naturally Worn; Illegible Information

  IT WAS REPORTED THAT THE SIZING INFORMATION WORN OFF TRIALS DUE TO MULTIPLE AUTOCLAVING/USAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14316861 ↗
• MalfunctionSep 29, 2021Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn

  IT WAS REPORTED THAT THE TRAIL HEAD IS WORN AND WILL NOT ATTACH TO TRIAL HANDLE. TRIAL HANDLE BALL BEARINGS AND WORN AND WILL NOT ALLOW ANY HEAD TRIALS TO BE ATTACHED. PLEASE SEND REPLACEMENTS TO CHARLESTON WAREHOUSE ATTN: FLOATER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12549899 ↗
• MalfunctionAug 27, 2019Material Twisted/Bent; Naturally Worn; Material Twisted/Bent; Naturally Worn

  TRIALS ARE WORN. PATIENT STATUS/OUTCOME/CONSEQUENCES: NO.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8934523 ↗
• MalfunctionAug 27, 2019Material Twisted/Bent; Naturally Worn; Material Twisted/Bent; Naturally Worn

  TRIALS ARE WORN. PATIENT STATUS / OUTCOME / CONSEQUENCES? NO.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8934522 ↗
• MalfunctionAug 27, 2019Material Twisted/Bent; Naturally Worn; Material Twisted/Bent; Naturally Worn

  TRIALS ARE WORN. PATIENT STATUS/ OUTCOME / CONSEQUENCES --> NO.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8934520 ↗
• MalfunctionNov 6, 2018Material Deformation; Material Deformation

  INSTRUMENTS DAMAGED DURING USE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8041217 ↗