DJO SURGICAL 935-44-260Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888912101714), received between Feb 7, 2019 and Mar 25, 2020 — classified as 2 injuries.

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

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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 25, 2020Break; Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - PATIENT FELL AND BROKE LINER.

  Patient problems: Fall

  MAUDE report 9878905 ↗
• InjuryFeb 7, 2019Device Dislodged or Dislocated

  SECOND REVISION SURGERY - PATIENT KEPT DISLOCATING; SO SURGEON SWITCHED TO A CONSTRAINED LINER AND HEAD.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8318699 ↗

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