Legacy™ Overdenture Abutment 8045-61Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10841307111511), received between May 11, 2018 and May 18, 2021 — classified as 3 injuries, 1 malfunction.

The most frequently reported specific device problem is “Fracture” (3 reports).

4 other recalls cover devices cleared under the same FDA submission (K061319); 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 18, 2021Fracture; Fracture

  PER COMPLAINT (B)(4) AFTER CLINICAL PROCEDURE, BROKEN OR FRACTURED COMPONENT WAS OBSERVED.

  Patient problems: Failure of Implant

  MAUDE report 11840826 ↗
• InjuryJan 30, 2020Loss of Osseointegration; Loss of Osseointegration

  PER COMPLAINT (B)(4), DURING CLINICAL PROCEDURE, PATIENT EXPERIENCED LOSS OR FAILURE OF IMPLANT TO INTEGRATE.

  Patient problems: Failure of Implant; Osteopenia/ Osteoporosis

  MAUDE report 9646147 ↗
• InjuryMay 11, 2018Fracture; Fracture

  ACCORDING TO THE COMPLAINT, (B)(4) DISTRIBUTOR REPORTS THE DENTAL IMPLANT ABUTMENT WAS BROKEN ONE YEAR AFTER FIXATION, CAUSING A REMOVAL OF THE IMPLANT. THIS IS A REPORTABLE SERIOUS INJURY.

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

  MAUDE report 7507647 ↗
• InjuryMay 11, 2018Fracture; Fracture

  ACCORDING TO THE COMPLAINT, (B)(4) DISTRIBUTOR REPORTS THE DENTAL IMPLANT ABUTMENT WAS BROKEN ONE YEAR AFTER FIXATION, CAUSING A REMOVAL OF THE IMPLANT. THIS IS A REPORTABLE SERIOUS INJURY.

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

  MAUDE report 7507590 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K061319. One submission often covers many models, so check the product and lot details in each record.

• Z-0010-2020 · Aug 7, 2018 · Terminated
  ImplantDirect simply RePlant Implant, size 4.3mmD x 13mmL, 4.3mmD Platform, REF 604313U, Rx, Sterile. The firm name on the label is Implant Direct Sybron Manufacturing LLC, Thousa
• Z-2376-2018 · May 18, 2018 · Terminated
  REPLANT 5.0mmD ABUTMENT, Part number 6050-52-60
• Z-2125-2017 · May 2, 2017 · Terminated
  Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD
• Z-2320-2016 · Jul 5, 2016 · Terminated
  RePlant Angled Abutment Part Number 6050-52-60