Skip to content

Legacy™ Implant Analog 8035-06DRecalls & 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
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841307122821), received between Mar 24, 2020 and Mar 24, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Missing Information” (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

  • Missing Information1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionMar 24, 2020Missing Information; Missing Information

    PER COMPLAINT (B)(4), DURING AN INTERNAL REVIEW, A PART WAS IDENTIFIED AS MISSING A LABEL.

    Patient problems: No Patient Involvement

    MAUDE report 9873304 ↗

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