TC-100 71143107Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 23596010387350), received between Jun 24, 2018 and Jun 24, 2018 — classified as 1 injury.

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

• InjuryJun 24, 2018Migration or Expulsion of Device; Migration or Expulsion of Device

  PRESENTED TO THE ED ON (B)(6) WITH RIGHT KNEE PAIN THAT HAD STARTED 3 DAYS PRIOR TO SEEKING HELP. REMOVAL OF DEEP HARDWARE RIGHT KNEE (3.5 CORTICAL SCREW X 1), ARTHROSCOPIC RIGHT KNEE LAVAGE FOR DRAINAGE OF SEPTIC ARTHRITIS, ARTHROSCOPIC RIGHT KNEE REMOVAL OF FOREIGN BODY (RETAINED INTRA-ARTICULAR SCREW WASHER), ARTHROSCOPIC RIGHT KNEE COMPLETE SYNOVECTOMY, FINDINGS - SIGNIFICANT ARTHROSIS MEDIAL COMPARTMENT WITH LARGE DEFECT, FROM INTRA-ARTICULAR SCREW TRACT, GROSS PURULENCE NOTED IN KNEE.

  Patient problems: Failure of Implant

  MAUDE report 7632769 ↗