ReActive ImplantRecalls & reported problems across all models

We found 22 models of ReActive Implant by Implant Direct Sybron Manufacturing LLC in the FDA's device registry (GUDID). Together they are named in 686 adverse event reports in the FDA's MAUDE database, received between Feb 24, 2018 and Aug 19, 2026 — classified as 679 injuries, 7 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (418 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported ReActive Implant problems

ReActive Implant models

22 models, most reported first. Each model has its own page with its reports, recalls and device details.

• ReActive® Implant 753710

  Implant, Endosseous, Root-Form
  165 reports
• ReActive® Implant 754710

  Implant, Endosseous, Root-Form
  117 reports
• ReActive® Implant 754210

  Implant, Endosseous, Root-Form
  82 reports
• ReActive® Implant 755710

  Implant, Endosseous, Root-Form
  60 reports
• ReActive® Implant 754713

  Implant, Endosseous, Root-Form
  39 reports
• ReActive® Implant 753713

  Implant, Endosseous, Root-Form
  34 reports
• ReActive® Implant 753711

  Implant, Endosseous, Root-Form
  32 reports
• ReActive® Implant 754711

  Implant, Endosseous, Root-Form
  30 reports
• ReActive® Implant 754211

  Implant, Endosseous, Root-Form
  25 reports
• ReActive® Implant 754708

  Implant, Endosseous, Root-Form
  23 reports
• ReActive® Implant 753708

  Implant, Endosseous, Root-Form
  21 reports
• ReActive® Implant 754213

  Implant, Endosseous, Root-Form
  19 reports
• ReActive® Implant 755708

  Implant, Endosseous, Root-Form
  9 reports
• ReActive® Implant 754208

  Implant, Endosseous, Root-Form
  8 reports
• ReActive® Implant 754716

  Implant, Endosseous, Root-Form
  8 reports
• ReActive® Implant 753716

  Implant, Endosseous, Root-Form
  5 reports
• ReActive® Implant 755713

  Implant, Endosseous, Root-Form
  3 reports
• ReActive® Implant 755711

  Implant, Endosseous, Root-Form
  2 reports
• ReActive® Implant 763710

  Implant, Endosseous, Root-Form
  1 report
• ReActive® Implant 764708

  Implant, Endosseous, Root-Form
  1 report
• ReActive® Implant 764710

  Implant, Endosseous, Root-Form
  1 report
• ReActive® Implant 765710

  Implant, Endosseous, Root-Form
  1 report

Recent ReActive Implant adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjuryAug 19, 2026Failure to Osseointegrate

  Failure to osseointegrate.

  Patient problems: Inadequate Osseointegration; No Clinical Signs, Symptoms or Conditions

  MAUDE report 50331414 ↗
• InjuryJun 10, 2026Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration; Unspecified Infection

  MAUDE report 25462083 ↗
• InjuryJun 4, 2026Separation Problem

  COMPONENT DOES NOT DISENGAGE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25402803 ↗
• InjuryJun 4, 2026Loss of Osseointegration

  LOSS OF OSSEOINTEGRATION.

  Patient problems: Inadequate Osseointegration; No Clinical Signs, Symptoms or Conditions

  MAUDE report 25402757 ↗
• InjuryJun 4, 2026Loss of Osseointegration

  LOSS OF OSSEOINTEGRATION.

  Patient problems: Inadequate Osseointegration; Inflammation; Osteopenia/ Osteoporosis; Unspecified Infection

  MAUDE report 25400028 ↗
• InjuryMay 28, 2026Failure to Osseointegrate

  PART NOT RETURNED.

  Patient problems: Inadequate Osseointegration; No Clinical Signs, Symptoms or Conditions

  MAUDE report 25322620 ↗
• InjuryMay 18, 2026Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration; No Clinical Signs, Symptoms or Conditions

  MAUDE report 25210254 ↗
• InjuryApr 13, 2026Loss of Osseointegration

  LOSS OF OSSEOINTEGRATION.

  Patient problems: Inadequate Osseointegration; No Clinical Signs, Symptoms or Conditions

  MAUDE report 24861228 ↗
• InjuryMar 30, 2026Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Bone Fracture(s); Inadequate Osseointegration

  MAUDE report 24736389 ↗
• InjuryMar 30, 2026Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Bone Fracture(s); Inadequate Osseointegration

  MAUDE report 24736196 ↗
• InjuryMar 30, 2026Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration; Inflammation

  MAUDE report 24735818 ↗
• InjuryMar 30, 2026Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Implant Pain; Inadequate Osseointegration

  MAUDE report 24735584 ↗
• InjuryMar 30, 2026Loss of Osseointegration

  LOSS OF OSSEOINTEGRATION.

  Patient problems: Bone Fracture(s); Inadequate Osseointegration

  MAUDE report 24728455 ↗
• InjuryMar 3, 2026Component Incompatible

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24503463 ↗
• InjuryMar 3, 2026Component Incompatible

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24503379 ↗

Other Implant Direct Sybron Manufacturing LLC products

• Legacy3 Implant75 models · 9,801 reports
• Legacy2 Implant78 models · 8,257 reports · 2 recalls
• simply InterActive Implant23 models · 4,946 reports
• simply Legacy2 Implant38 models · 3,319 reports
• RePlant Implant20 models · 2,351 reports
• SIMPLY ICONIC Implant39 models · 2,189 reports
• Legacy4 Implant58 models · 1,786 reports
• Legacy1 Implant27 models · 1,635 reports