NobelSpeedy® 32148 (UDI 07332747159820)Recalls & reported problems
Nobel Biocare AB · NobelSpeedy® Groovy RP 4.0x10mm · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
Quick summary
This Nobel Biocare NobelSpeedy implant is a screw placed in the jawbone to hold a replacement tooth. Of its 1,740 reports, 1 involves a death and 1,717 involve an injury, and most describe the implant failing to fuse with the bone or later losing that bond. Some mention the implant moving from its intended position, infection and abscesses. 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
- 1,769
- Deaths reported
- 1
- Injuries reported
- 1,746
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1,769 adverse event reports that list this exact device (DI 07332747159820), received between Nov 1, 2021 and Sep 30, 2026 — classified as 1 death, 1,746 injuries, 22 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (922 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Osseointegrate922
- Loss of Osseointegration681
- Osseointegration Problem62
- Patient Device Interaction Problem32
- Adverse Event Without Identified Device or Use Problem26
- Fracture24
- Device Markings/Labelling Problem4
- Difficult to Remove4
Patient problems
- Failure of Implant1,142
- Unspecified Infection309
- No Clinical Signs, Symptoms or Conditions301
- Pain166
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available77
- Abscess34
- Numbness26
- Implant Pain20
Recent adverse event reports
The 25 most recent of 1,769 reports, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Loss of Osseointegration
Patient problems: Pain
MAUDE report 50953831 ↗InjurySep 30, 2026Loss of Osseointegration
Patient problems: Pain
MAUDE report 50953827 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50796357 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50796355 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: Aspiration/Inhalation
MAUDE report 50796010 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: Aspiration/Inhalation
MAUDE report 50796009 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: Aspiration/Inhalation
MAUDE report 50796003 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: Aspiration/Inhalation
MAUDE report 50796000 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: Aspiration/Inhalation
MAUDE report 50795922 ↗InjurySep 16, 2026Loss of Osseointegration
Patient problems: Aspiration/Inhalation
MAUDE report 50795915 ↗InjurySep 15, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780498 ↗InjurySep 15, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780497 ↗InjurySep 15, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780496 ↗InjurySep 15, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50780492 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764328 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764321 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764308 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764303 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744132 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744131 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744104 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744102 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744100 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744099 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744096 ↗
Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM43,616 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM40,404 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM27,400 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,621 reports
- STRAUMANN BONE LEVEL TAPERED IMPLANT SLA Titanium BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM25,298 reports
- Straumann® Dental Implant System Roxolid® SLA Impl. SLA Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM23,448 reports
- 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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