Scorpio 72-25-1112Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327029819), received between Sep 14, 2022 and Feb 15, 2023 — classified as 2 injuries.

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

1 other recall cover devices cleared under the same FDA submission (K051977); 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 15, 2023Fracture; Fracture

  IT WAS REPORTED THAT THE PATIENT'S LEFT KNEE WAS REVISED DUE TO THE POST OF THE PS INSERT FRACTURING. AN 11X12 SCORPIO FLEX PS INSERT WAS EXCHANGED FOR ANOTHER 11X12 SCORPIO FLEX PS INSERT.

  Patient problems: Insufficient Information

  MAUDE report 16376962 ↗
• InjurySep 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT REPORTED A PRIMARY RIGHT KNEE REPLACEMENT IN 2013. PATIENT STATED "SORENESS" BUT NO ADDITIONAL ISSUES OR CONCERNS. PATIENT WOULD LIKE TO KNOW IF PARTS ARE SUBJECT TO A RECALL.

  Patient problems: Pain

  MAUDE report 15417591 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K051977. One submission often covers many models, so check the product and lot details in each record.

• 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