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Scorpio 73-3110Recalls & reported problems

Howmedica Osteonics Corp. · Universal Dome Patella · Class 2 · Implant

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

2 FDA recall records name this device's identifier, 2 still open.

7 other recalls cover devices cleared under the same FDA submission (K051948, K052917, K243817, K252898, K972967); 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. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jul 30, 2026Open, Classified

    Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

    Z-3206-2026 · Root cause: Process change control · FDA record ↗

  2. Dec 1, 2023Open, Classified

    Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated levels of oxidation. Oxidation within UHMWPE can have an impact on its material properties.

    Z-0893-2024 · Root cause: Nonconforming Material/Component · FDA record ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K051948, K052917, K243817, K252898, K972967. One submission often covers many models, so check the product and lot details in each record.

  • 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-0894-2024 · Dec 1, 2023 · Open, Classified
    SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
  • Z-0895-2024 · Dec 1, 2023 · Open, Classified
    SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508
  • Z-0897-2024 · Dec 1, 2023 · Open, Classified
    SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
  • Z-0896-2024 · Dec 1, 2023 · Open, Classified
    SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3708
  • Z-0900-2024 · Dec 1, 2023 · Open, Classified
    Scorpio NRG Tibial Brg Insert Assy -Intended for knee replacement Part Number: 82-2-0910
  • Z-0606-2012 · Aug 17, 2011 · Terminated
    Eius Unicompartmental Knee System Stryker Howmedica Osteonics Corp. Howmedica International S. de R.L., Raheen Business Park, Limerick, Ireland. Intended for use in Unicompartment

Other PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER devices

All PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.