Skip to content

BioHorizons TD-2507Recalls & reported problems

Biohorizons Implant Systems, Inc · 2.5mm Tapered Surgical Drill, Grey, 7.5mm · Class 1

Adverse event reports
6
Deaths reported
0
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00847236021993), received between May 8, 2025 and Aug 14, 2026 — classified as 6 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (6 reports).

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. How this data works · Data updated Oct 13, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 1 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 2 reportsMar 2026: 1 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 2 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate6

Patient problems

  • Insufficient Information6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 14, 2026Failure to Osseointegrate

    Implant failed to osseointegrate.

    Patient problems: Insufficient Information

    MAUDE report 50256370 ↗
  • InjuryAug 10, 2026Failure to Osseointegrate

    Implant failed to osseointegrate.

    Patient problems: Insufficient Information

    MAUDE report 50190390 ↗
  • InjuryMar 5, 2026Failure to Osseointegrate

    IMPLANT FAILED TO OSSEOINTEGRATE.

    Patient problems: Insufficient Information

    MAUDE report 24519460 ↗
  • InjuryFeb 16, 2026Failure to Osseointegrate

    IMPLANT FAILED TO OSSEOINTEGRATE.

    Patient problems: Insufficient Information

    MAUDE report 24345741 ↗
  • InjuryFeb 6, 2026Failure to Osseointegrate

    IMPLANT FAILED TO OSSEOINTEGRATE.

    Patient problems: Insufficient Information

    MAUDE report 24279533 ↗
  • InjuryMay 8, 2025Failure to Osseointegrate; Failure to Osseointegrate

    IMPLANT FAILED TO OSSEOINTEGRATE.

    Patient problems: Insufficient Information

    MAUDE report 21984276 ↗

Other Accessories, Implant, Dental, Endosseous devices

All Accessories, Implant, Dental, Endosseous devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.