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Legacy™3 Implant 863710Recalls & reported problems

Implant Direct Sybron Manufacturing LLC · 3.7mmD x 10mmL, 3.5mmD Platform · Class 2 · Implant

All models of Legacy3 Implant (75)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
23
Deaths reported
0
Injuries reported
23
Recalls naming it
0

Summary

The FDA's MAUDE database contains 23 adverse event reports that list this exact device (DI 10841307102458), received between Feb 19, 2018 and Sep 8, 2023 — classified as 23 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (12 reports).

11 other recalls cover devices cleared under the same FDA submission (K090234); 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

Device problems

  • Failure to Osseointegrate12
  • Loss of Osseointegration8
  • Device Issue1
  • Fracture1
  • Positioning Failure1

Patient problems

  • Failure of Implant23
  • Inflammation5
  • No Consequences Or Impact To Patient5
  • Unspecified Infection5
  • Osteopenia/ Osteoporosis4
  • Pain3
  • Granuloma2
  • Fibrosis1

Recent adverse event reports

The 23 most recent of 23 reports, in the reporter's own words as published by the FDA.

  • InjurySep 8, 2023Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant

    MAUDE report 17710855 ↗
  • InjuryAug 3, 2023Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; Granuloma; Inflammation; Unspecified Infection

    MAUDE report 17451361 ↗
  • InjuryFeb 17, 2023Positioning Failure; Positioning Failure

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

    Patient problems: Failure of Implant

    MAUDE report 16397801 ↗
  • InjuryFeb 17, 2023Loss of Osseointegration; Loss of Osseointegration

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED LOSS OF IMPLANT TO OSSEOINTEGRATE

    Patient problems: Failure of Implant; Osteopenia/ Osteoporosis; Pain

    MAUDE report 16397375 ↗
  • InjuryFeb 14, 2022Loss of Osseointegration; Loss of Osseointegration

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED LOSS OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant

    MAUDE report 13530104 ↗
  • InjuryJan 11, 2022Fracture; Fracture

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PRODUCT FRACTURE IS OBSERVED.

    Patient problems: Failure of Implant

    MAUDE report 13226212 ↗
  • InjuryDec 29, 2021Loss 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

    MAUDE report 13108118 ↗
  • InjuryFeb 12, 2021Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; Granuloma

    MAUDE report 11321402 ↗
  • InjuryJan 29, 2021Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant; Pain; Unspecified Infection

    MAUDE report 11250621 ↗
  • InjuryDec 30, 2020Failure to Osseointegrate; Failure to Osseointegrate

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

    Patient problems: Failure of Implant

    MAUDE report 11094569 ↗
  • InjuryJul 21, 2020Failure to Osseointegrate; Failure to Osseointegrate

    AS PER COMPLAINT (B)(4) A DENTAL IMPLANT DISPLAYED A FAILURE OF OSSEOINTEGRATION AND THE IMPLANT WAS EXPLANTED.

    Patient problems: Failure of Implant; Inflammation

    MAUDE report 10302072 ↗
  • InjuryApr 17, 2020Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; Osteopenia/ Osteoporosis

    MAUDE report 9971685 ↗
  • InjuryApr 1, 2020Loss of Osseointegration; Loss of Osseointegration

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED LOSS OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; Fibrosis; Inflammation; Unspecified Infection

    MAUDE report 9909641 ↗
  • InjuryJan 30, 2020Loss of Osseointegration; Loss of Osseointegration

    PER COMPLAINT (B)(4), AFTER CLINICAL PROCEDURE, PATIENT EXPERIENCED FAILURE OF IMPLANT TO OSSEOINTEGRATE.

    Patient problems: Failure of Implant; No Information

    MAUDE report 9646090 ↗
  • InjuryJan 17, 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; No Consequences Or Impact To Patient

    MAUDE report 9600222 ↗
  • InjuryJan 16, 2020Loss of Osseointegration; Loss of Osseointegration

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

    Patient problems: Failure of Implant; Osteopenia/ Osteoporosis

    MAUDE report 9595299 ↗
  • InjuryNov 12, 2019Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), DURING POST OPERATIVE CHECK, PATIENT EXPERIENCED LOSS OR FAILURE OF IMPLANT TO INTEGRATE.

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

    MAUDE report 9309038 ↗
  • InjuryOct 9, 2019Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), AFTER PROSTHETIC TREATMENT, PATIENT EXPERIENCED LOSS OR FAILURE OF IMPLANT TO INTEGRATE.

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

    MAUDE report 9171383 ↗
  • InjurySep 17, 2019Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), DURING POST OPERATIVE CHECK, PATIENT EXPERIENCED LOSS OR FAILURE OF IMPLANT TO INTEGRATE.

    Patient problems: Failure of Implant; Inflammation; Unspecified Infection

    MAUDE report 9075274 ↗
  • InjurySep 11, 2019Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), DURING POST OPERATIVE CHECK PATIENT EXPERIENCED FAILURE OF IMPLANT TO INTEGRATE AND IMPLANT WAS EXTRUDED DUE TO FLUCTUATION.

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

    MAUDE report 8987329 ↗
  • InjurySep 10, 2019Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), DURING POST OPERATIVE CHECK, PATIENT EXPERIENCED FAILURE OR LOSS OF IMPLANT TO INTEGRATE. THE IMPLANT WAS REMOVED DUE TO INFECTION.

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

    MAUDE report 8979871 ↗
  • InjuryAug 21, 2019Loss of Osseointegration; Loss of Osseointegration

    PER COMPLAINT (B)(4), PATIENT HAD EXPERIENCED FAILURE OF IMPLANT TO INTEGRATE.

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

    MAUDE report 8914100 ↗
  • InjuryFeb 19, 2018Device Issue; Device Issue

    CUSTOMER REPORTED THAT THE IMPLANT ENTERED THE MANDIBULAR CANAL CAUSING NUMBNESS OF THE LIP AND CHIN OF THE PATIENT.

    Patient problems: Failure of Implant

    MAUDE report 7281183 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K090234. One submission often covers many models, so check the product and lot details in each record.

  • Z-1157-2020 · Oct 11, 2019 · Terminated
    Implant Direct, CE 0086, REF: 855710, Legacy 3 Impant, Surface: SBM, Qty:1, Size:5.7mmD x 10mmL, 5.7mmD Platform, RxOnly, Sterile R,
  • Z-1041-2020 · Oct 7, 2019 · Terminated
    Legacy 3 Implant, Size: 4.2mmD x 13mmL, 3.5mmD Platform, REF: 864213
  • Z-0364-2020 · Aug 9, 2019 · Terminated
    Implant Direct, REF: 833708, Legacy 2 Implant, Surface: HA, 3.7mmD x 8mmL, 3.5mmD Platform, RxOnly, Sterile R, Made in USA Dental Implants
  • Z-0018-2020 · Aug 8, 2018 · Terminated
    ImplantDirect Legacy 3 Implant, REF 855216, SBM implant assembly, 2mmD x 16mmL, 4.5mmD platform, Rx, Sterile. The mislabeled model/part number on the vial cap is 835216. The re
  • Z-1167-2018 · Jan 19, 2018 · Terminated
    SwishTapered Implant Intended for use in support for fixed bridgework.
  • Z-0185-2018 · Oct 10, 2017 · Terminated
    ImplantDirect Legacy(TM) 3 Implant, 13MM L, REF 864713 This Legacy implant is a two-piece implant for one-stage or two-stage surgical procedures. These implants are intended for
  • Z-0007-2018 · Jul 21, 2017 · Terminated
    Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.
  • Z-1112-2017 · Dec 12, 2016 · Terminated
    SwishTapered Implant
  • Z-0961-2017 · Nov 28, 2016 · Terminated
    GoDirect Screw-Retaining Top Part Numbers: 4500-61
  • Z-1920-2018 · Nov 15, 2016 · Terminated
    ImplantDirect Legacy 4 Implant, 5.7mmD x 5.7mmD Platform, Part 885708, Rx, Sterile. The incorrect cap label shows part 855708, 5.7mmD Platform, 8mmL.
  • Z-1267-2016 · Mar 4, 2016 · Terminated
    The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that compose a two-piece implant system. GoDirect Implants Part Numbe

Other Implant, Endosseous, Root-Form devices

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Sources and updates

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