Scorpio 82-3-0910Recalls & reported problems
Howmedica Osteonics Corp. · Tibial Bearing Insert · Class 2 · Implant
All models of Scorpio (107)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04546540364494), received between Sep 27, 2019 and Jun 20, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Fracture” (2 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
Device problems
- Fracture2
- Break1
Patient problems
- Injury1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 20, 2022Fracture; Fracture
IT HAS BEEN REPORTED "IN A PATIENT WITH NRG KNEE REPLACEMENT, THE X3 INSERT WAS BROKEN, THE PATIENT REQUIRED A SECOND OPERATION."
Patient problems: Insufficient Information
MAUDE report 14748429 ↗InjurySep 27, 2019Break; Fracture; Break; Fracture
IT WAS REPORTED THAT PATIENT UNDERWENT TOTAL KNEE ARTHROPLASTY 2 YEARS AGO. THE PATIENT COMPLAINED OF INSTABILITY AND VISITED TO HOSPITAL. X-RAY SHOWED HYPER EXTENSION OF PATIENT KNEE. REVISION SURGERY WAS PERFORMED ON (B)(6) 2019 AND SURGEON FOUND SCORPIO NRG POST OF INSERT WAS BROKEN. THE BROKEN INSERT WAS REPLACED AND REVISION SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Injury
MAUDE report 9131167 ↗
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, ClassifiedSCORPIO 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, ClassifiedALL 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, ClassifiedScorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0908
- Z-1634-2015 · Aug 15, 2014 · TerminatedStryker 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 · TerminatedScorpio 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 · TerminatedScorpio 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-0470-2010 · Oct 2, 2009 · TerminatedScorpio 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-0472-2010 · Oct 2, 2009 · TerminatedScorpio 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-0474-2010 · Oct 2, 2009 · TerminatedScorpio 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-0475-2010 · Oct 2, 2009 · TerminatedScorpio 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 · TerminatedScorpio 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-0473-2010 · Oct 2, 2009 · TerminatedScorpio 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-1141-2010 · Aug 20, 2007 · TerminatedHowmedica Osteonics Corp., Scorpio NRG Femoral Size 7 Right; Knee prosthesis (Stryker France). Product Code: 814407R. Mahwah, NJ
Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices
- ATTUNE 1506-00-005Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER589 reports
- ATTUNE 1506-00-004Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER580 reports
- JOURNEY 74012812Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER502 reports
- JOURNEY 74011856Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER438 reports
- PERSONA™ 42-5099-094-00Zimmer, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER406 reports
- JOURNEY 74011857Smith & Nephew, Inc. · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER388 reports
- ATTUNE 1506-00-007Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER288 reports
- ATTUNE 1506-00-003Depuy (Ireland) · PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER271 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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