Skip to content

Legacy™ Implant Closed-Tray Transfer 8530-05Recalls & reported problems

Implant Direct Sybron Manufacturing LLC · Class 1 · Implant

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841307121442), received between Apr 27, 2022 and Apr 27, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Loss of Osseointegration” (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

Device problems

  • Loss of Osseointegration1

Patient problems

  • Failure of Implant1
  • Fibrosis1
  • Granuloma1
  • Osteopenia/ Osteoporosis1
  • Unspecified Infection1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryApr 27, 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; Fibrosis; Granuloma; Osteopenia/ Osteoporosis; Unspecified Infection

    MAUDE report 14220464 ↗

Other Accessories, Implant, Dental, Endosseous devices

All Accessories, Implant, Dental, Endosseous devices →

Sources and updates

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