PHYSICA TT 6521.14.060Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08033390174299), received between Mar 23, 2023 and May 10, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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 16, 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.

• InjuryMay 10, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  KNEE REVISION SURGERY DUE TO LOOSENING OF THE PHYSICA TT FIX. TIBIAL TRAY #5, COMMERCIAL CODE 652114050 - LOT #2202412 - STER. #2200182 THE COMPLAINT SOURCE REPORTED THAT THE IMPLANT HAD TILTED. THE REVISION SURGERY DATE WAS (B)(6) 2023, THE DATE OF THE PREVIOUS SURGERY IS (B)(6) 2023. PATIENT IS FEMALE DATE OF BIRTH - (B)(6)1951. APPROX. HEIGHT = 165.00CM. APPROX WEIGHT =69KG. OCCUPATION - RETIRED. ACTIVITY LEVEL = STRONGLY REDUCED. BMI =25.34.

  Patient problems: Joint Laxity

  MAUDE report 16900702 ↗
• InjuryMar 23, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  KNEE REVISION SURGERY DUE TO LOOSENING OF THE TIBIAL IMPLANT WITH PRODUCT CODE 6521.14.060 LOT 2023630 STER. 2100042. THE COMPLAINT SOURCE REPORTED THAT THE IMPLANT HAD TILTED. THE REVISION SURGERY DATE IS (B)(6) 2023, THE DATE OF THE PREVIOUS SURGERY IS (B)(6) 2021. PATIENT IS MALE, BORN ON (B)(6) 1947. THIS EVENT OCCURRED IN FRANCE.

  Patient problems: Insufficient Information

  MAUDE report 16597700 ↗