Scorpio 72-4-0714Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327034462), received between Dec 18, 2019 and Dec 18, 2019 — classified as 1 injury.

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

10 other recalls cover devices cleared under the same FDA submission (K243817, K994128); 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 18, 2019Unstable; Unstable

  THE PATIENT REQUIRED A TS LINER CHANGE AT THE SAME TIME AS AN EXTENSOR MECHANISM REPAIR DUE TO INSTABILITY AND RECURRENT DISLOCATION OF THE PATELLA TENDON, AS WELL AS THE FEMUR ON THE INSERT. THE SCORPIO TS WAS IMPLANTED IN 2010, AND REVISED A KNEE APPROX 20 YEARS OLD ( NO RECORDS AVAIL ). THE TS WAS FINE FOR 4 YEARS, THEN BECAME UNSTABLE AFTER A FALL, AND STARTED TO RECURRENTLY DISLOCATE. THE PT DID NOT CONSENT TO REVISION SURGERY UNTIL HIS OPERATION YESTERDAY. THE SURGEON STATED THE PATIENTS INSTABILITY WAS MADE WORSE BY THE FACT HE HAD NO PATELLA. ( PREVIOUS PATELLECTOMY).

  Patient problems: Fall; Injury; Joint Dislocation

  MAUDE report 9488730 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K243817, K994128. 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-0880-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT. Intended for knee replacement Part Number: 72-4-7518
• Z-0877-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT-Intended for knee replacement Part Number:72-4-7512
• Z-0875-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321
• Z-0876-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0510
• Z-0878-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7514
• Z-0882-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7524
• Z-0881-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-7521
• Z-0879-2024 · Dec 1, 2023 · Open, Classified
  SCORPIO TS TIB INSERT -Intended for knee replacment Part Number: 72-4-7516