Scorpio 82-3-0918Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 04546540364524), received between Mar 6, 2020 and Jul 22, 2021 — classified as 4 injuries.

The most frequently reported specific device problem is “Fracture” (4 reports).

13 other recalls cover devices cleared under the same FDA submission (K030978, K243817); 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 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJul 22, 2021Fracture; Fracture

  IT WAS REPORTED THAT FIRST REVISION SURGERY WAS PERFORMED IN 2019 BECAUSE OF POST BREAKAGE OF NRG INSERT. AFTER 1.5 YEARS, SAME PATIENT HAD PROBLEM OF NRG POST OF INSERT PART. THE POST OF INSERT WAS BROKEN TWICE.

  Patient problems: Ambulation or Postural Difficulties; Insufficient Information

  MAUDE report 12209044 ↗
• InjuryApr 2, 2020Fracture; Fracture

  AFTER 2ND REVISION SURGERY FOR SPECIFIED IMPLANT TKR DONE ON (B)(6) 2016, IMPLANT BROKE AGAIN ON (B)(6) 2017. 3RD REVISION SURGERY DONE (B)(6) 2018.

  Patient problems: Injury

  MAUDE report 9915652 ↗
• InjuryApr 2, 2020Fracture; Fracture

  AFTER 1ST SURGERY FOR SPECIFIED IMPLANT TKR IN 2014, IMPLANT BROKE AGAIN ON (B)(6) 2016 . 2ND REVISION SURGERY DONE (B)(6) 2016.

  Patient problems: Injury

  MAUDE report 9915645 ↗
• InjuryMar 6, 2020Fracture; Fracture

  MY SELF IS SUFFERING VERY PAINFUL CONDITION BECAUSE OF YOUR POOR QUALITY PRODUCT. LAST YEAR INSTALL YOUR COMPANY PRODUCT "TIBIAL BEARING" WHICH IS DAMAGE INTERNALLY. WHEN WE DISCUSS WITH MANAGEMENT STAFF AND DOCTOR THEY SAID THAT'S NOT OUR FAULT IT'S STRYKER MATERIALS FAULT. THE PATIENT WAS REVISED ON (B)(6) 2020. THE INSERT WITH A BROKEN POST WAS REMOVED. A NEW SCORPIO NRG SIZE 9 18MM PS INSERT WAS THEN IMPLANTED.

  Patient problems: Injury; Pain

  MAUDE report 9800184 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K030978, K243817. One submission often covers many models, so check the product and lot details in each record.

• Z-3206-2026 · Jul 30, 2026 · Open, Classified
  SCORPIO C-DOME PATELLA 73-2710 73-2910 SCORPIO U-DOME PATELLA 73-3110 73-3508 73-3708 73-3710 73-3910 Orthopaedic implant components manufactured from UHMWPE (polyet
• Z-3197-2026 · Jul 30, 2026 · Open, Classified
  ALL POLY CONSTRAINED INSERT 54MM 69-2854 NRG KNEE CR 82-2-0512 82-2-0518 82-2-0912 NRG KNEE P/S 82-3-0318 SCORPIO + MOBILE BEARING PCS 78-5-0910 SCORPIO C-DOME PAT
• Z-0899-2024 · Dec 1, 2023 · Open, Classified
  Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0908
• Z-1634-2015 · Aug 15, 2014 · Terminated
  Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in USA Sterile. For use in total reconstructive replacement of
• Z-0473-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Posterior Stabilized Femoral, #3 Left; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is utilize
• Z-0474-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Posterior Stabilized Femoral. # 4 left/right; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is
• Z-0471-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Cruciate Retaining Femoral, Right # 7; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is utilize
• Z-0472-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Cruciate Retaining Femoral, Left # 8; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is utilized
• Z-0477-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Posterior Stabilized Femoral, #9 left; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is utilize
• Z-0475-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Posterior Stabilized Femoral, # 5 Left; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07340. The Scorpio Femoral Components are a knee component that is utiliz
• Z-0476-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Posterior Stabilized Femoral, # 7 left/right; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is
• Z-0470-2010 · Oct 2, 2009 · Terminated
  Scorpio NRG Cruciate Retaining Femoral, Left/Right # 5; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 07430. The Scorpio Femoral Components are a knee component that is ut
• Z-1141-2010 · Aug 20, 2007 · Terminated
  Howmedica Osteonics Corp., Scorpio NRG Femoral Size 7 Right; Knee prosthesis (Stryker France). Product Code: 814407R. Mahwah, NJ