DJO SURGICAL 315-0B-717Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00888912114011), received between Jan 25, 2017 and Feb 24, 2023 — classified as 9 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 24, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - DUE TO THE PATIENT WAS HAVING CHRONIC RIGHT KNEE PAIN.

  Patient problems: Implant Pain

  MAUDE report 16440513 ↗
• InjuryFeb 22, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY DUE TO INSTABILITY.

  Patient problems: Joint Laxity

  MAUDE report 16424128 ↗
• InjuryApr 13, 2022Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - PATIENT FELL AND DISLOCATED KNEE.

  Patient problems: Fall; Joint Dislocation

  MAUDE report 14105063 ↗
• InjuryAug 19, 2021Loose or Intermittent Connection

  REVISION SURGERY - PATIENT WAS REVISED DUE TO LAXITY OF THE JOINT.

  Patient problems: Insufficient Information

  MAUDE report 12345127 ↗
• InjuryJan 13, 2021Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - PATIENT WAS UNSTABLE AND COMPLAINING OF PAIN. SURGEON INCREASED POLY TO A 19MM.

  Patient problems: Balance Problems; Pain

  MAUDE report 11163294 ↗
• InjuryMay 1, 2019Microbial Contamination of Device

  REVISION SURGERY - DUE TO THE PATIENT ACQUIRING A POST OPERATIVE INFECTION. THE SURGEON DID A WASH OUT AND CHANGED THE POLY.

  Patient problems: Unspecified Infection

  MAUDE report 8570742 ↗
• InjuryJul 7, 2017Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO THE PATIENT HAVING AN INFECTION; THE SURGEON SWAPPED OUT THE POLY.

  Patient problems: Unspecified Infection

  MAUDE report 6694513 ↗
• InjuryFeb 2, 2017Insufficient Device Problem Information

  REVISION SURGERY - DUE TO THE PATIENT HAVING A POST-OP INFECTION. THE SURGEON WENT BACK IN AND DID AN IRRIGATION & DRAINAGE, THEN WENT AHEAD AND SWAPPED OUT THE POLY INSERT.

  Patient problems: Unspecified Infection

  MAUDE report 6298303 ↗
• InjuryJan 25, 2017Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO AN IRRIGATION AND DRAINAGE WASH OUT AND THE REPLACEMENT OF THE POLY.

  Patient problems: No Code Available

  MAUDE report 6277326 ↗

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.