Replace SelectRecalls & reported problems across all models
Nobel Biocare AB · 107 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 33,616
- Deaths reported
- 0
- Injuries reported
- 33,305
- Recalls
- 0
We found 107 models of Replace Select by Nobel Biocare AB in the FDA's device registry (GUDID). Together they are named in 33,616 adverse event reports in the FDA's MAUDE database, received between Oct 31, 2018 and Sep 30, 2026 — classified as 33,305 injuries, 311 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (15,570 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 Replace Select problems
Device problems
- Failure to Osseointegrate15,570
- Loss of Osseointegration14,633
- Osseointegration Problem1,623
- Fracture681
- Adverse Event Without Identified Device or Use Problem501
- Migration164
- Patient Device Interaction Problem120
- Insufficient Device Problem Information107
Patient problems
- Failure of Implant25,926
- No Clinical Signs, Symptoms or Conditions4,994
- Pain4,118
- Unspecified Infection3,667
- Numbness938
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available550
- Abscess292
- Inflammation197
Replace Select models
107 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Replace Select™ 29413IMPLANT, ENDOSSEOUS, ROOT-FORM2,648 reports
- Replace Select™ 29413IMPLANT, ENDOSSEOUS, ROOT-FORM2,142 reports
- Replace Select™ 37306IMPLANT, ENDOSSEOUS, ROOT-FORM1,910 reports
- Replace Select™ 29414IMPLANT, ENDOSSEOUS, ROOT-FORM1,378 reports
- Replace Select™ 29414IMPLANT, ENDOSSEOUS, ROOT-FORM1,374 reports
- Replace Select™ 37301IMPLANT, ENDOSSEOUS, ROOT-FORM1,130 reports
- Replace Select™ 29423IMPLANT, ENDOSSEOUS, ROOT-FORM953 reports
- Replace Select™ 29423IMPLANT, ENDOSSEOUS, ROOT-FORM892 reports
- Replace Select™ 29401IMPLANT, ENDOSSEOUS, ROOT-FORM847 reports
- Replace Select™ 37311IMPLANT, ENDOSSEOUS, ROOT-FORM841 reports
- Replace Select™ 29401IMPLANT, ENDOSSEOUS, ROOT-FORM832 reports
- Replace Select™ 37305IMPLANT, ENDOSSEOUS, ROOT-FORM794 reports
- Replace Select™ 36107IMPLANT, ENDOSSEOUS, ROOT-FORM718 reports
- Replace Select™ 37306IMPLANT, ENDOSSEOUS, ROOT-FORM627 reports
- Replace Select™ 29402IMPLANT, ENDOSSEOUS, ROOT-FORM599 reports
- Replace Select™ 37308IMPLANT, ENDOSSEOUS, ROOT-FORM595 reports
- Replace Select™ 37300IMPLANT, ENDOSSEOUS, ROOT-FORM566 reports
- Replace Select™ 36106IMPLANT, ENDOSSEOUS, ROOT-FORM560 reports
- Replace Select™ 37307IMPLANT, ENDOSSEOUS, ROOT-FORM532 reports
- Replace Select™ 37303IMPLANT, ENDOSSEOUS, ROOT-FORM526 reports
- Replace Select™ 36107IMPLANT, ENDOSSEOUS, ROOT-FORM518 reports
- Replace Select™ 37310IMPLANT, ENDOSSEOUS, ROOT-FORM514 reports
- Replace Select™ 29402IMPLANT, ENDOSSEOUS, ROOT-FORM511 reports
- Replace Select™ 37302IMPLANT, ENDOSSEOUS, ROOT-FORM462 reports
- Replace Select™ 36106IMPLANT, ENDOSSEOUS, ROOT-FORM438 reports
- Replace Select™ 36105IMPLANT, ENDOSSEOUS, ROOT-FORM436 reports
- Replace Select™ 29424IMPLANT, ENDOSSEOUS, ROOT-FORM396 reports
- Replace Select™ 36105IMPLANT, ENDOSSEOUS, ROOT-FORM393 reports
- Replace Select™ 37301IMPLANT, ENDOSSEOUS, ROOT-FORM374 reports
- Replace Select™ 37308IMPLANT, ENDOSSEOUS, ROOT-FORM340 reports
- Replace Select™ 36109IMPLANT, ENDOSSEOUS, ROOT-FORM324 reports
- Replace Select™ 29415IMPLANT, ENDOSSEOUS, ROOT-FORM319 reports
- Replace Select™ 29424IMPLANT, ENDOSSEOUS, ROOT-FORM315 reports
- Replace Select™ 37311IMPLANT, ENDOSSEOUS, ROOT-FORM311 reports
- Replace Select™ 36108IMPLANT, ENDOSSEOUS, ROOT-FORM294 reports
- Replace Select™ 37307IMPLANT, ENDOSSEOUS, ROOT-FORM292 reports
- Replace Select™ 36290IMPLANT, ENDOSSEOUS, ROOT-FORM286 reports
- Replace Select™ 36108IMPLANT, ENDOSSEOUS, ROOT-FORM279 reports
- Replace Select™ 37302IMPLANT, ENDOSSEOUS, ROOT-FORM260 reports
- Replace Select™ 37303IMPLANT, ENDOSSEOUS, ROOT-FORM253 reports
- Replace Select™ 29415IMPLANT, ENDOSSEOUS, ROOT-FORM248 reports
- Replace Select™ 36286IMPLANT, ENDOSSEOUS, ROOT-FORM234 reports
- Replace® Select 28952IMPLANT, ENDOSSEOUS, ROOT-FORM218 reports
- Replace Select™ 36104IMPLANT, ENDOSSEOUS, ROOT-FORM216 reports
- Replace Select™ 36291IMPLANT, ENDOSSEOUS, ROOT-FORM198 reports
- Replace Select™ 36109IMPLANT, ENDOSSEOUS, ROOT-FORM194 reports
- Replace Select™ 37305IMPLANT, ENDOSSEOUS, ROOT-FORM194 reports
- Replace Select™ 37315IMPLANT, ENDOSSEOUS, ROOT-FORM187 reports
- Replace Select™ 37310IMPLANT, ENDOSSEOUS, ROOT-FORM175 reports
- Replace Select™ 37300IMPLANT, ENDOSSEOUS, ROOT-FORM175 reports
- Replace Select™ 36104IMPLANT, ENDOSSEOUS, ROOT-FORM170 reports
- Replace® Select 28951IMPLANT, ENDOSSEOUS, ROOT-FORM160 reports
- Replace Select™ 37316IMPLANT, ENDOSSEOUS, ROOT-FORM157 reports
- Replace Select™ 36287IMPLANT, ENDOSSEOUS, ROOT-FORM150 reports
- Replace Select™ 32949IMPLANT, ENDOSSEOUS, ROOT-FORM146 reports
- Replace Select™ 37312IMPLANT, ENDOSSEOUS, ROOT-FORM146 reports
- Replace® Select 28953IMPLANT, ENDOSSEOUS, ROOT-FORM145 reports
- Replace Select™ 29403IMPLANT, ENDOSSEOUS, ROOT-FORM132 reports
- Replace Select™ 37313IMPLANT, ENDOSSEOUS, ROOT-FORM128 reports
- Replace® Select 28956IMPLANT, ENDOSSEOUS, ROOT-FORM123 reports
- Replace Select™ 37312IMPLANT, ENDOSSEOUS, ROOT-FORM115 reports
- Replace Select™ 36292IMPLANT, ENDOSSEOUS, ROOT-FORM111 reports
- Replace Select™ 36286IMPLANT, ENDOSSEOUS, ROOT-FORM106 reports
- Replace® Select 28957IMPLANT, ENDOSSEOUS, ROOT-FORM96 reports
- Replace Select™ 29403IMPLANT, ENDOSSEOUS, ROOT-FORM95 reports
- Replace Select™ 36290IMPLANT, ENDOSSEOUS, ROOT-FORM92 reports
- Replace Select™ 36291IMPLANT, ENDOSSEOUS, ROOT-FORM86 reports
- Replace Select™ 37309IMPLANT, ENDOSSEOUS, ROOT-FORM84 reports
- Replace Select™ 29425IMPLANT, ENDOSSEOUS, ROOT-FORM76 reports
- Replace® Select 28954IMPLANT, ENDOSSEOUS, ROOT-FORM74 reports
- Replace Select™ 32949IMPLANT, ENDOSSEOUS, ROOT-FORM69 reports
- Replace Select™ 37317IMPLANT, ENDOSSEOUS, ROOT-FORM68 reports
- Replace Select™ 37313IMPLANT, ENDOSSEOUS, ROOT-FORM66 reports
- Replace Select™ 37304IMPLANT, ENDOSSEOUS, ROOT-FORM66 reports
- Replace Select™ 36287IMPLANT, ENDOSSEOUS, ROOT-FORM65 reports
- Replace® Select 28946IMPLANT, ENDOSSEOUS, ROOT-FORM62 reports
- Replace Select™ 36111IMPLANT, ENDOSSEOUS, ROOT-FORM60 reports
- Replace® Select 28958IMPLANT, ENDOSSEOUS, ROOT-FORM58 reports
- Replace Select™ 29425IMPLANT, ENDOSSEOUS, ROOT-FORM57 reports
- Replace Select™ 37309IMPLANT, ENDOSSEOUS, ROOT-FORM54 reports
- Replace® Select 28948IMPLANT, ENDOSSEOUS, ROOT-FORM50 reports
- Replace® Select 28947IMPLANT, ENDOSSEOUS, ROOT-FORM48 reports
- Replace Select™ 32950IMPLANT, ENDOSSEOUS, ROOT-FORM47 reports
- Replace Select™ 37316IMPLANT, ENDOSSEOUS, ROOT-FORM45 reports
- Replace Select™ 36285IMPLANT, ENDOSSEOUS, ROOT-FORM44 reports
- Replace Select™ 37318IMPLANT, ENDOSSEOUS, ROOT-FORM44 reports
- Replace Select™ 32950IMPLANT, ENDOSSEOUS, ROOT-FORM42 reports
- Replace Select™ 36110IMPLANT, ENDOSSEOUS, ROOT-FORM37 reports
- Replace® Select 28949IMPLANT, ENDOSSEOUS, ROOT-FORM36 reports
- Replace Select™ 37317IMPLANT, ENDOSSEOUS, ROOT-FORM34 reports
- Replace Select™ 37314IMPLANT, ENDOSSEOUS, ROOT-FORM34 reports
- Replace® Select 28959IMPLANT, ENDOSSEOUS, ROOT-FORM32 reports
- Replace Select™ 36288IMPLANT, ENDOSSEOUS, ROOT-FORM28 reports
- Replace Select™ 37304IMPLANT, ENDOSSEOUS, ROOT-FORM27 reports
- Replace Select™ 36288IMPLANT, ENDOSSEOUS, ROOT-FORM24 reports
- Replace Select™ 36292IMPLANT, ENDOSSEOUS, ROOT-FORM24 reports
- Replace Select™ 36289IMPLANT, ENDOSSEOUS, ROOT-FORM24 reports
- Replace Select™ 37315IMPLANT, ENDOSSEOUS, ROOT-FORM24 reports
- Replace Select™ 36285IMPLANT, ENDOSSEOUS, ROOT-FORM22 reports
- Replace Select™ 36111IMPLANT, ENDOSSEOUS, ROOT-FORM22 reports
Recent Replace Select adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954493 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954492 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954490 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954488 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50954469 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50954467 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Unspecified Infection
MAUDE report 50954324 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Unspecified Infection
MAUDE report 50954316 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954303 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954297 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: Abscess
MAUDE report 50954293 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: Abscess
MAUDE report 50954291 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954016 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954015 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953681 ↗
Other Nobel Biocare AB products
- NobelActive56 models · 152,066 reports
- NobelReplace120 models · 138,221 reports · 15 recalls
- NobelParallel54 models · 132,525 reports
- NobelActive TiUltra28 models · 82,969 reports
- NobelParallel Conical Connection TiUltra27 models · 68,868 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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