Scorpio 81-4405RRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327029390), received between Dec 17, 2018 and Dec 17, 2018 — classified as 1 injury.

The most frequently reported specific device problem is “Unstable” (1 report).

11 other recalls cover devices cleared under the same FDA submission (K030978); 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.

• InjuryDec 17, 2018Unstable; Unstable

  IT WAS REPORTED THAT THE PATIENT'S RIGHT KNEE WAS REVISED DUE TO INSTABILITY. NO POSSIBLE CAUSE OR CONTRIBUTOR FOR INSTABILITY WAS REPORTED TO THE REP. THE FEMORAL COMPONENT, INSERT, AND CEMENTED TIBIA WERE REVISED. NONE OF THE RECORDS ACCESSIBLE TO REP CONFIRMED THE MANUFACTURER OF THE CEMENT. REP REPORTED THAT X-RAYS, MEDICAL RECORDS, AND ADDITIONAL INFORMATION ARE NOT AVAILABLE.

  Patient problems: Injury

  MAUDE report 8170207 ↗

Recalls under the same FDA submission

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

• 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-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-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-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-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-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-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-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