DJO SURGICAL 120-01-726Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888912108393), received between May 13, 2019 and Aug 13, 2024 — classified as 2 injuries.

1 other recall cover devices cleared under the same FDA submission (K113756); 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.

• InjuryAug 13, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY - DUE TO PATELLA TENDON RUPTURE

  Patient problems: Muscle/Tendon Damage

  MAUDE report 19978331 ↗
• InjuryMay 13, 2019Appropriate Device Problem Term/Code Not Available

  REVISION SURGERY - DUE TO THE PATELLA JOINT BEING OVER-STUFFED. THE SURGEON RE-CUT THE PATELLA.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8605765 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K113756. One submission often covers many models, so check the product and lot details in each record.

• Z-0626-2024 · Oct 5, 2023 · Completed
  REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2