Legacy™4 Implant 883711Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10841307103264), received between Jun 21, 2019 and Dec 22, 2020 — classified as 2 injuries.

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

2 other recalls cover devices cleared under the same FDA submission (K192221); 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.

• InjuryDec 22, 2020Failure to Osseointegrate; Failure to Osseointegrate

  PER COMPLAINT (B)(4), DURING CLINICAL PROCEDURE, PATIENT EXPERIENCED LACK OF PRIMARY STABILITY.

  Patient problems: Failure of Implant; Inflammation; Osteopenia/ Osteoporosis; Pain; Unspecified Infection

  MAUDE report 11053396 ↗
• InjuryJun 21, 2019Break; Break

  PER COMPLAINT (B)(4), IT WAS REPORTED THAT A PATIENT'S DENTAL CROWN HAD COME OFF. IT WAS DISCOVERED THROUGH A PERIAPICAL RADIOGRAPH THAT THE PATIENT HAD A BROKEN ABUTMENT AND DENTAL IMPLANT. THE IMPLANT COULD NOT BE SAVED DUE TO THE DAMAGE. THE IMPLANT WAS REMOVED AND WILL BE REPLACED ONCE THE AREA IS HEALED.

  Patient problems: Failure of Implant; No Consequences Or Impact To Patient

  MAUDE report 8722915 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K192221. One submission often covers many models, so check the product and lot details in each record.

• Z-0198-2022 · Sep 23, 2021 · Open, Classified
  ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,
• Z-0197-2022 · Sep 23, 2021 · Open, Classified
  ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,