STRAUMANN BONE LEVEL TAPERED IMPLANTRecalls & reported problems across all models
Institut Straumann AG · 39 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one STRAUMANN BONE LEVEL TAPERED IMPLANT model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 308,650
- Deaths reported
- 0
- Injuries reported
- 308,650
- Recalls
- 1
We found 39 models of STRAUMANN BONE LEVEL TAPERED IMPLANT by Institut Straumann AG in the FDA's device registry (GUDID). Together they are named in 308,650 adverse event reports in the FDA's MAUDE database, received between Aug 28, 2019 and Sep 30, 2026 — classified as 308,650 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (242,482 reports).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
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
STRAUMANN BONE LEVEL TAPERED IMPLANT recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jul 16, 2026Open, Classified
Bone Level Tapered (BLT) Implant, D 4.1mm RC, SLActive 14mm, Roxolid, Loxim may inadvertently contain implants that are 12mm in length instead of 14mm as the labeling would suggest.
Z-2935-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported STRAUMANN BONE LEVEL TAPERED IMPLANT problems
Device problems
- Failure to Osseointegrate242,482
- Loss of Osseointegration49,941
- Adverse Event Without Identified Device or Use Problem12,946
- Difficult to Insert1,897
- Fracture1,869
- Separation Failure348
- Unintended Movement110
- Difficult to Remove102
Patient problems
- No Clinical Signs, Symptoms or Conditions163,036
- Fibrosis82,864
- Pain51,574
- Unspecified Infection36,232
- Inflammation21,242
- Tissue Damage19,389
- Swelling/ Edema15,130
- Hemorrhage/Blood Loss/Bleeding11,518
STRAUMANN BONE LEVEL TAPERED IMPLANT models
39 models, most reported first. Each model has its own page with its reports, recalls and device details.
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM20,463 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM19,746 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM19,554 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM14,666 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM14,465 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM13,574 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM11,195 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM9,862 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM9,777 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM9,478 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM6,161 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM1 recall4,384 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM4,321 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM2,789 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM2,486 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM1,898 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM1,635 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM951 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM644 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM575 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM571 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM478 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM459 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM454 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM406 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM339 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM334 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM212 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM205 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM168 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM165 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM155 reports
- Straumann Bone Level Tapered Implant SLActive Roxolid BLIMPLANT, ENDOSSEOUS, ROOT-FORM94 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLIMPLANT, ENDOSSEOUS, ROOT-FORM76 reports
Recent STRAUMANN BONE LEVEL TAPERED IMPLANT 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
The clinician reports the implant was inserted 2026(b)(6) in FDI 17. On 2026(b)(6) non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950328 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted (b)(6)2025 in FDI 14. On (b)(6)2026, non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950326 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2026(b)(6) in FDI 24. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950324 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2026(b)(6) in FDI 36. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950323 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2026(b)(6) in FDI 17. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950321 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted (b)(6)2026 in FDI 47. On (b)(6)2026, non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950317 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted (b)(6) 2025 in FDI 36. On (b)(6) 2026, non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950316 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2025(b)(6) in FDI 32. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950313 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted (b)(6) 2025 in FDI 44. On (b)(6) 2026, non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950312 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2025(b)(6) in FDI 25. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950311 ↗InjurySep 30, 2026Failure to Osseointegrate
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950310 ↗InjurySep 30, 2026Loss of Osseointegration
The clinician reports the implant was inserted 2024(b)(6) in FDI 46. On 2026(b)(6), loss of osseointegration was verified. The device was forwarded to the manufacturer. There were no patient operative or post-operative complications reported.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950309 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2025(b)(6) in FDI 47. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950308 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2025(b)(6) in FDI 16. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950303 ↗InjurySep 30, 2026Failure to Osseointegrate
The clinician reports the implant was inserted 2026(b)(6) in FDI 46. On 2026(b)(6), non-osseointegration was verified. The device was forwarded to the manufacturer. There were no reported patient injuries or complications.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950302 ↗
Other Institut Straumann AG products
- Straumann Dental Implant System Roxolid SLA Impl.80 models · 377,342 reports
- STRAUMANN DENTAL IMPLANT SYSTEM128 models · 98,339 reports
- MODIFICATION TO ITI DENTAL IMPLANT SYSTEM42 models · 80,770 reports
- Straumann BLX Implant System60 models · 78,869 reports
- BL, 04.1 MM RC, SLACTIVE 8MM, TIZR AND 10MM, 12, 14MM14 models · 39,692 reports
- Straumann BLC and TLC Implants153 models · 20,568 reports
- ITI DENTAL IMPLANT SYSTEM60 models · 19,402 reports
- Small Diameter Implant System5 models · 16,170 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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