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NobelSpeedy® 32151 (UDI 07332747159851)Recalls & reported problems

Nobel Biocare AB · NobelSpeedy® Groovy RP 4.0x15mm · Class 2 · Implant

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Quick summary

This NobelSpeedy dental implant is a root-form implant placed in the jaw to support a replacement tooth. Its 1,563 reports mostly describe the implant failing to bond with the jawbone or being lost, and some mention infection, pain or numbness. The reports include 1,552 injuries and no deaths. 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
1,592
Deaths reported
0
Injuries reported
1,581
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1,592 adverse event reports that list this exact device (DI 07332747159851), received between Oct 29, 2021 and Sep 30, 2026 — classified as 1,581 injuries, 11 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (880 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

Nov 2023: 24 reportsDec 2023: 14 reportsJan 2024: 12 reportsFeb 2024: 32 reportsMar 2024: 30 reportsApr 2024: 22 reportsMay 2024: 14 reportsJun 2024: 18 reportsJul 2024: 54 reportsAug 2024: 16 reportsSep 2024: 34 reportsOct 2024: 33 reportsNov 2024: 32 reportsDec 2024: 32 reportsJan 2025: 24 reportsFeb 2025: 52 reportsMar 2025: 46 reportsApr 2025: 4 reportsMay 2025: 0 reportsJun 2025: 2 reportsJul 2025: 96 reportsAug 2025: 52 reportsSep 2025: 18 reportsOct 2025: 32 reportsNov 2025: 32 reportsDec 2025: 53 reportsJan 2026: 29 reportsFeb 2026: 32 reportsMar 2026: 38 reportsApr 2026: 30 reportsMay 2026: 42 reportsJun 2026: 32 reportsJul 2026: 28 reportsAug 2026: 11 reportsSep 2026: 32 reportsOct 2026: 0 reports20242025202696
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate880
  • Loss of Osseointegration518
  • Osseointegration Problem80
  • Patient Device Interaction Problem46
  • Adverse Event Without Identified Device or Use Problem24
  • Fracture20
  • Material Deformation6
  • Migration6

Patient problems

  • Failure of Implant977
  • No Clinical Signs, Symptoms or Conditions297
  • Unspecified Infection192
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available139
  • Pain88
  • Numbness50
  • Implant Pain28
  • Bone Fracture(s)14

Recent adverse event reports

The 25 most recent of 1,592 reports, in the reporter's own words as published by the FDA.

Other IMPLANT, ENDOSSEOUS, ROOT-FORM devices

All IMPLANT, ENDOSSEOUS, ROOT-FORM devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page