DJO SURGICAL 931-40-256Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00888912099707), received between Jun 30, 2017 and Jul 3, 2024 — classified as 7 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

1 other recall cover devices cleared under the same FDA submission (K072154); 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 18, 2026.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryJul 3, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - DUE TO METAL ON METAL, CHANGED TO A STANDER LINER.

  Patient problems: Insufficient Information

  MAUDE report 19672427 ↗
• InjuryMar 7, 2022Crack; Loose or Intermittent Connection; Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY: ORIGINALLY THE LINER WAS REMOVED TO PUT IN A MP9 40MMID/5MM OFFSET LINER. DURING THE IMPACTION OF THAT THE PELVIS HAS CRACKED. SURGEON THEN DECIDED TO REMOVE THE CUP AND 2 SCREWS AND REPLACE IT ALL WITH BIOMET. THE CLP STEM WAS ALSO REMOVED WITH THE ORIGINAL 40MM/-4 BIOPIC HEAD AS THE STEM WAS LOOSE CAUSING DISLOCATION.

  Patient problems: Insufficient Information

  MAUDE report 13684826 ↗
• InjuryAug 22, 2019Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 8923596 ↗
• InjuryAug 15, 2019Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - POSSIBLE INFECTION HENCE COMPLETED IRRIGATION AND DRAINAGE WASHOUT AND SWAPPED POLY. (SURGEON USED A DIFFERENT VENDOR FOR THE HEAD).

  Patient problems: Fluid Discharge; Unspecified Infection

  MAUDE report 8898152 ↗
• InjuryMay 9, 2019Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO THE PATIENT'S ACETABULAR COMPONENT SHIFTING VERTICALLY CAUSING PAIN AND LEG SHORTENING. THE SURGEON REMOVED AND REPLACED ALL IMPLANTS EXCEPT FOR THE STEM.

  Patient problems: Pain

  MAUDE report 8596459 ↗
• InjuryOct 4, 2018Device Dislodged or Dislocated

  REVISION SURGERY - DUE TO A DISLOCATION.

  Patient problems: Failure of Implant

  MAUDE report 7935068 ↗
• InjuryJun 30, 2017Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY: DUE TO THE PATIENT HAVING AN INFECTION; THE SURGEON PERFORMED A WASHOUT AND HEAD AND POLY EXCHANGE.

  Patient problems: Unspecified Infection

  MAUDE report 6683082 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K072154. One submission often covers many models, so check the product and lot details in each record.

• Z-1130-2014 · Feb 7, 2014 · Terminated
  FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell to replicate the kinematics of a natural hi