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SwishPlant® Implant 904810Recalls & reported problems

Implant Direct Sybron Manufacturing LLC · 4.8mmD x 10mmL, 4.8mmD Platform · Class 2 · Implant

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10841307105947), received between Sep 5, 2019 and Nov 21, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K081396); 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 Osseointegrate1
  • Loss of Osseointegration1

Patient problems

  • Failure of Implant2
  • No Consequences Or Impact To Patient1
  • No Information1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 21, 2019Loss of Osseointegration; Loss of Osseointegration

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

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

    MAUDE report 9351899 ↗
  • InjurySep 5, 2019Failure to Osseointegrate; Failure to Osseointegrate

    PER COMPLAINT (B)(4), A PATIENT'S DENTAL IMPLANT FAILED TO OSSEOINTEGRATE. THE IMPLANT WAS REMOVED. NO ADDITIONAL ADVERSE PATIENT CONSEQUENCES WERE REPORTED.

    Patient problems: Failure of Implant; No Information

    MAUDE report 8967760 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K081396. One submission often covers many models, so check the product and lot details in each record.

  • Z-1126-2020 · Jan 9, 2019 · Terminated
    SwishPlus Implant 5.7mmD x 8mmL, SBM 6.5mmD Platform, Part Number 925708
  • Z-1168-2018 · Jan 19, 2018 · Terminated
    SwishPlus Implant Intended for use in support for fixed bridgework.
  • Z-0396-2016 · Oct 28, 2015 · Terminated
    DGDE, DirectGuide Drill Extender. Instrument for use with dental implants. A manufactured device that adds a 6mm extension for a 25mm and 28mm tissue height capability suitable

Other Implant, Endosseous, Root-Form devices

All Implant, Endosseous, Root-Form devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page