NobelSpeedy® 32152 (UDI 07332747159868)Recalls & reported problems
Nobel Biocare AB · NobelSpeedy® Groovy RP 4.0x18mm · 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 804 adverse event reports, 792 describing injuries and no deaths. Most describe the implant failing to bond with the jawbone or losing that bond later, and some mention infection, pain and numbness. 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
- 828
- Deaths reported
- 0
- Injuries reported
- 816
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 828 adverse event reports that list this exact device (DI 07332747159868), received between Nov 1, 2021 and Sep 17, 2026 — classified as 816 injuries, 12 malfunctions.
The most frequently reported specific device problem is “Failure to Osseointegrate” (528 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
- Failure to Osseointegrate528
- Loss of Osseointegration206
- Osseointegration Problem34
- Patient Device Interaction Problem26
- Fracture18
- Adverse Event Without Identified Device or Use Problem8
- Activation, Positioning or Separation Problem2
- Contamination /Decontamination Problem2
Patient problems
- Failure of Implant548
- No Clinical Signs, Symptoms or Conditions124
- Unspecified Infection98
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available90
- Pain74
- Numbness30
- Inflammation6
- Abscess4
Recent adverse event reports
The 25 most recent of 828 reports, in the reporter's own words as published by the FDA.
InjurySep 17, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50811941 ↗InjurySep 17, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50811939 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764409 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764404 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764327 ↗InjurySep 14, 2026Osseointegration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50764294 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744137 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744124 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744122 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744118 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744112 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744111 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744109 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744108 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744091 ↗InjurySep 11, 2026Loss of Osseointegration
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50744090 ↗InjurySep 10, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50724420 ↗InjurySep 10, 2026Failure to Osseointegrate
Patient problems: Unspecified Infection
MAUDE report 50724419 ↗InjurySep 10, 2026Loss of Osseointegration
Patient problems: Unspecified Infection
MAUDE report 50724407 ↗InjurySep 10, 2026Loss of Osseointegration
Patient problems: Unspecified Infection
MAUDE report 50724403 ↗InjurySep 10, 2026Loss of Osseointegration
Patient problems: Unspecified Infection
MAUDE report 50724394 ↗InjurySep 10, 2026Loss of Osseointegration
Patient problems: Unspecified Infection
MAUDE report 50724389 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50700946 ↗InjurySep 9, 2026Loss of Osseointegration
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50700943 ↗InjuryAug 27, 2026Failure to Osseointegrate
Failure to osseointegrate.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 50487220 ↗
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- STRAUMANN BONE LEVEL TAPERED IMPLANT SLActive Roxolid BLInstitut Straumann AG · IMPLANT, ENDOSSEOUS, ROOT-FORM22,320 reports
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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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