Scorpio 73-20-3508Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327014570), received between Jan 29, 2019 and Jan 29, 2019 — classified as 1 injury.

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

9 other recalls cover devices cleared under the same FDA submission (K051977, K052917); 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.

• InjuryJan 29, 2019Break; Break

  ON (B)(6) 2013, TKA PROCEDURE DONE. THE PRODUCTS #81-4406R, #OR-7115-0005, #82-7-0512,#73-20-3508 WERE IMPLANTED IN PATIENT. ON (B)(6) 2019, PERFORMING TKA RE-REPLACEMENT SURGERY WITH MCL (MEDIAL COLLATERAL LIGAMENT) FAILURE. THE REPLACEMENT IMPLANT IS COMPETITOR 360. IMPLANTED PEG WAS BROKEN AND THE 73-20-3508 X3 PATELLA UNIVERSAL DOME WAS BROKEN ALSO.

  Patient problems: Damage to Ligament(s); Injury

  MAUDE report 8285946 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K051977, K052917. 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-0897-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3710
• Z-0893-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3110
• Z-0895-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3508
• 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-0894-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73-3308
• 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
• Z-0911-2010 · Feb 17, 2006 · Terminated
  Scorpio X3 UHMPWE Tibial Inserts and Scorpio X3 UHMWPE Patellar Components, multiple sizes, Stryker Orthopaedics, Mahwah, NJ. Intended to be used with cemented or cementless compo