NobelSpeedy® 32154 (UDI 07332747159882)Recalls & reported problems
Nobel Biocare AB · NobelSpeedy® Groovy WP 5.0x8.5mm · Class 2 · Implant
All models of NobelSpeedy (88)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Nobel Biocare NobelSpeedy dental implant has 146 FDA adverse event reports, with no deaths and 143 injuries. Most describe the implant failing to fuse with the jawbone or losing that bond. Patients were most often reported with implant failure, and some mention infection, abscesses or pain. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 148
- Deaths reported
- 0
- Injuries reported
- 145
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 148 adverse event reports that list this exact device (DI 07332747159882), received between Nov 26, 2021 and Sep 10, 2026 — classified as 145 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Loss of Osseointegration” (88 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Loss of Osseointegration88
- Failure to Osseointegrate42
- Adverse Event Without Identified Device or Use Problem8
- Osseointegration Problem6
- Device Markings/Labelling Problem2
- Malposition of Device2
Patient problems
- Failure of Implant87
- No Clinical Signs, Symptoms or Conditions30
- Unspecified Infection29
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available10
- Pain10
- Abscess6
- Inflammation4
- Fistula2
Recent adverse event reports
The 25 most recent of 148 reports, in the reporter's own words as published by the FDA.
InjurySep 10, 2026Failure to Osseointegrate
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50724349 ↗InjurySep 10, 2026Failure to Osseointegrate
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50724348 ↗InjuryJul 2, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25699262 ↗InjuryJul 2, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25699247 ↗InjuryJun 26, 2026Failure to Osseointegrate
InjuryJun 25, 2026Loss of Osseointegration
InjuryJun 25, 2026Loss of Osseointegration
InjuryJun 24, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25615139 ↗InjuryJun 24, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25615134 ↗InjuryJun 5, 2026Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 25417965 ↗InjuryJun 5, 2026Failure to Osseointegrate
FAILURE TO OSSEOINTEGRATE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 25417093 ↗InjuryJun 4, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 25402096 ↗InjuryJun 4, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 25402087 ↗InjuryMay 27, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25309294 ↗InjuryMay 27, 2026Loss of Osseointegration
LOSS OF OSSEOINTEGRATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25309272 ↗InjuryMay 27, 2026Loss of Osseointegration
InjuryMay 27, 2026Loss of Osseointegration
InjuryMar 30, 2026Loss of Osseointegration
InjuryMar 30, 2026Loss of Osseointegration
InjuryMar 26, 2026Loss of Osseointegration
InjuryMar 26, 2026Loss of Osseointegration
InjuryMar 10, 2026Loss of Osseointegration
InjuryMar 10, 2026Loss of Osseointegration
InjuryJan 30, 2026Failure to Osseointegrate
InjuryJan 30, 2026Failure to Osseointegrate
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,267 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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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