DJO SURGICAL 935-28-248Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912101400), received between Jan 7, 2019 and Jan 7, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 7, 2019Device Dislodged or Dislocated

  REVISION SURGERY - DUE TO THE PATIENT DISLOCATING. THE SURGEON IMPLANTED A CONSTRAINED LINER IN THE PATIENT TO KEEP HIM FROM DISLOCATING AGAIN.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8223042 ↗

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