NobelSpeedy® 32141 (UDI 07332747159752)Recalls & reported problems
Nobel Biocare AB · NobelSpeedy® Groovy WP 6.0x10mm · Class 2 · Implant
- Adverse event reports
- 22
- Deaths reported
- 0
- Injuries reported
- 22
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 07332747159752), received between Apr 6, 2023 and Jul 27, 2026 — classified as 22 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (16 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
- Loss of Osseointegration16
- Failure to Osseointegrate4
- Device Markings/Labelling Problem2
Patient problems
- Failure of Implant6
- No Clinical Signs, Symptoms or Conditions6
- Unspecified Infection6
- Abscess2
- Pain2
Recent adverse event reports
The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.
InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50031874 ↗InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50031871 ↗InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50030327 ↗InjuryJul 27, 2026Loss of Osseointegration
Loss of osseointegration.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50030326 ↗InjuryMay 27, 2026Loss of Osseointegration
InjuryMay 27, 2026Loss of Osseointegration
InjuryMay 6, 2026Failure to Osseointegrate
InjuryMay 6, 2026Failure to Osseointegrate
InjuryFeb 16, 2026Loss of Osseointegration
InjuryFeb 16, 2026Loss of Osseointegration
InjuryDec 9, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryDec 9, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryAug 8, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryAug 8, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 14, 2025Loss of Osseointegration; Loss of Osseointegration
InjuryJan 14, 2025Loss of Osseointegration; Loss of Osseointegration
InjurySep 18, 2024Loss of Osseointegration; Loss of Osseointegration
IMPLANT FAILED DUE TO A LOSS OF OSSEOINTEGRATION.
Patient problems: Failure of Implant
MAUDE report 20251430 ↗InjurySep 18, 2024Loss of Osseointegration; Loss of Osseointegration
IMPLANT FAILED DUE TO A LOSS OF OSSEOINTEGRATION.
Patient problems: Failure of Implant
MAUDE report 20250814 ↗InjuryApr 15, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IMPLANT FAILED DUE TO USABILITY - WRONG PART USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19111262 ↗InjuryApr 15, 2024Device Markings/Labelling Problem; Device Markings/Labelling Problem
IMPLANT FAILED DUE TO USABILITY - WRONG PART USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19109410 ↗InjuryApr 6, 2023Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT FAILED DUE TO A FAILURE TO OSSEOINTEGRATE.
Patient problems: Failure of Implant
MAUDE report 16692542 ↗InjuryApr 6, 2023Failure to Osseointegrate; Failure to Osseointegrate
IMPLANT FAILED DUE TO A FAILURE TO OSSEOINTEGRATE.
Patient problems: Failure of Implant
MAUDE report 16692540 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.