NobelActive TiUltraRecalls & reported problems across all models
Nobel Biocare AB · 28 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 82,969
- Deaths reported
- 2
- Injuries reported
- 81,765
- Recalls
- 0
We found 28 models of NobelActive TiUltra by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 82,969 adverse event reports in the FDA's MAUDE database, received between Oct 29, 2021 and Sep 30, 2026 — classified as 2 deaths, 81,765 injuries, 1,202 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (57,447 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
Reports received per month, all models
Most reported NobelActive TiUltra problems
Device problems
- Failure to Osseointegrate57,447
- Loss of Osseointegration11,160
- Osseointegration Problem7,012
- Adverse Event Without Identified Device or Use Problem1,979
- Patient Device Interaction Problem1,586
- Fracture1,100
- Migration757
- Difficult to Insert406
Patient problems
- Failure of Implant52,471
- No Clinical Signs, Symptoms or Conditions22,765
- Unspecified Infection6,226
- Pain5,301
- Inflammation1,284
- Abscess1,208
- Implant Pain1,053
- Numbness912
NobelActive TiUltra models
28 models, most reported first. Each model has its own page with its reports, recalls and device details.
- NobelActive® TiUltra™ 300251IMPLANT, ENDOSSEOUS, ROOT-FORM10,351 reports
- NobelActive® TiUltra™ 300252IMPLANT, ENDOSSEOUS, ROOT-FORM1 death7,572 reports
- NobelActive® TiUltra™ 300246IMPLANT, ENDOSSEOUS, ROOT-FORM7,532 reports
- NobelActive® TiUltra™ 300245IMPLANT, ENDOSSEOUS, ROOT-FORM7,505 reports
- NobelActive® TiUltra™ 300253IMPLANT, ENDOSSEOUS, ROOT-FORM6,998 reports
- NobelActive® TiUltra™ 300247IMPLANT, ENDOSSEOUS, ROOT-FORM6,675 reports
- NobelActive® TiUltra™ 300257IMPLANT, ENDOSSEOUS, ROOT-FORM5,414 reports
- NobelActive® TiUltra™ 300250IMPLANT, ENDOSSEOUS, ROOT-FORM4,471 reports
- NobelActive® TiUltra™ 300256IMPLANT, ENDOSSEOUS, ROOT-FORM3,012 reports
- NobelActive® TiUltra™ 300244IMPLANT, ENDOSSEOUS, ROOT-FORM2,803 reports
- NobelActive® TiUltra™ 300264IMPLANT, ENDOSSEOUS, ROOT-FORM2,751 reports
- NobelActive® TiUltra™ 300254IMPLANT, ENDOSSEOUS, ROOT-FORM2,633 reports
- NobelActive® TiUltra™ 300258IMPLANT, ENDOSSEOUS, ROOT-FORM2,503 reports
- NobelActive® TiUltra™ 300248IMPLANT, ENDOSSEOUS, ROOT-FORM2,228 reports
- NobelActive® TiUltra™ 300263IMPLANT, ENDOSSEOUS, ROOT-FORM1,656 reports
- NobelActive® TiUltra™ 300265IMPLANT, ENDOSSEOUS, ROOT-FORM1,443 reports
- NobelActive® TiUltra™ 300259IMPLANT, ENDOSSEOUS, ROOT-FORM1,422 reports
- NobelActive® TiUltra™ 300262IMPLANT, ENDOSSEOUS, ROOT-FORM1,009 reports
- NobelActive® TiUltra™ 300241IMPLANT, ENDOSSEOUS, ROOT-FORM946 reports
- NobelActive® TiUltra™ 300240IMPLANT, ENDOSSEOUS, ROOT-FORM1 death832 reports
- NobelActive® TiUltra™ 300242IMPLANT, ENDOSSEOUS, ROOT-FORM800 reports
- NobelActive® TiUltra™ 300266IMPLANT, ENDOSSEOUS, ROOT-FORM626 reports
- NobelActive® TiUltra™ 300255IMPLANT, ENDOSSEOUS, ROOT-FORM461 reports
- NobelActive® TiUltra™ 300260IMPLANT, ENDOSSEOUS, ROOT-FORM458 reports
- NobelActive® TiUltra™ 300249IMPLANT, ENDOSSEOUS, ROOT-FORM384 reports
- NobelActive® TiUltra™ 300243IMPLANT, ENDOSSEOUS, ROOT-FORM216 reports
- NobelActive® TiUltra™ 300267IMPLANT, ENDOSSEOUS, ROOT-FORM156 reports
- NobelActive® TiUltra™ 300261IMPLANT, ENDOSSEOUS, ROOT-FORM112 reports
Recent NobelActive TiUltra adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954482 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954474 ↗InjurySep 30, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954407 ↗InjurySep 30, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954405 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954403 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954401 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954394 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954392 ↗InjurySep 30, 2026Migration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954389 ↗InjurySep 30, 2026Migration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954387 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954196 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954191 ↗InjurySep 30, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954187 ↗InjurySep 30, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954186 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954182 ↗
Other Nobel Biocare AB products
- NobelActive56 models · 152,066 reports
- NobelReplace120 models · 138,221 reports · 15 recalls
- NobelParallel54 models · 132,525 reports
- NobelParallel Conical Connection TiUltra27 models · 68,868 reports
- Replace Select107 models · 33,616 reports
- NobelReplace Conical Connection TiUltra15 models · 31,165 reports
- NobelSpeedy88 models · 24,246 reports
- Brånemark System141 models · 19,899 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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