DJO SURGICAL 315-0B-714Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00888912114004), received between Dec 20, 2017 and Jul 21, 2022 — classified as 5 injuries.

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 (K140830); 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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryJul 21, 2022Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - PATIENT KNEE BECAME INFECTED, ALL IMPLANTS REMOVED, ANTIBIOTIC SPACER INSERTED.

  Patient problems: Unspecified Infection

  MAUDE report 15077208 ↗
• InjuryJul 18, 2022Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - PATIENT INCISION OPEN UP SO WASHED IT OUT AND CHANGE THE POLY.

  Patient problems: Wound Dehiscence

  MAUDE report 15048438 ↗
• InjuryApr 27, 2021Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - INFECTION AND WASHOUT WITH POLYSWAP.

  Patient problems: Unspecified Infection

  MAUDE report 11732017 ↗
• InjuryFeb 25, 2021Device Dislodged or Dislocated; Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO TIBIA SUBLUXATION.

  Patient problems: Insufficient Information

  MAUDE report 11380036 ↗
• InjuryDec 20, 2017Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - THE SURGEON WENT IN TO CLEAN OUT SCAR TISSUE AND SWAPPED OUT THE POLY WHILE HE WAS IN THERE.

  Patient problems: No Code Available; Scar Tissue

  MAUDE report 7135851 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K140830. One submission often covers many models, so check the product and lot details in each record.

• Z-0165-2016 · Sep 16, 2015 · Terminated
  Exprt Precision System: Revision Knee, Model Number 160-010-726/738 For use with the Exprt Knee System in total knee arthroplasty to replace the native patella.