Scorpio 72-25-0912Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327029710), received between Jun 13, 2019 and Jun 13, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 13, 2019Break; Unstable; Break; Unstable

  IT WAS REPORTED THAT THE PATIENT'S LEFT KNEE WAS REVISED AFTER PATIENT COMPLAINT OF A FEELING OF LOOSENESS IN THE KNEE. INTRA- OPERATIVELY, THE POST OF THE PS INSERT WAS OBSERVED TO BE BROKEN OFF. ALL PIECES OF THE DEVICE WERE REMOVED AND A DEVICE OF THE SAME CATALOG NUMBER WAS IMPLANTED. REP REPORTED THAT NO FURTHER INFORMATION WILL BE AVAILABLE.

  Patient problems: Injury

  MAUDE report 8695347 ↗

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