TOETAC HT-00002Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327356359), received between Aug 20, 2020 and Aug 20, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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 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.

• InjuryAug 20, 2020Migration; Migration

  IT WAS REPORTED THAT: " INCISION AND EXPLORATION OF 2ND PHALANX PROXIMAL TO MIDDLE PHALANGEAL JOINT WAS EXPLORED. UPON JOINT EXPLORATION IMPLANT COULD NOT INITIALLY BE LOCATED. FLEXOR DIGITORUM TENDON WAS INCISED TO EXPLORE IF IMPLANT WAS FLOATING FREELY WITHIN THE JOINT. IMPLANT WAS NOT FOUND STILL. UPON EXPLORING THE MIDDLE PHALANX IMPLANT WAS FOUND PROTRUDING, INTACT, FROM MIDDLE PHALANX WITH PROXIMAL PORTION OF IMPLANT EXPOSED. IMPLANT WAS REMOVED FROM THE MIDDLE PHALANX USING THE TOE TAC DRIVER HANDLE. FLEXOR DIGITORUM TENDON WAS REPAIRED WITH SUTURES. PROXIMAL INTERPHALANGEAL JOINT WAS ARTICULATED AND STABILIZED WITH A 0.045" K-WIRE AND INCISION WAS CLOSED WITH SUTURES."

  Patient problems: Inflammation; Injury

  MAUDE report 10434260 ↗