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NobelParallel™ 37971 (UDI 07332747161267)Recalls & reported problems

Nobel Biocare AB · NobelParallel™ Conical Connection RP 4.3x8.5mm · Class 2 · Implant

Quick summary

This NobelParallel Conical Connection dental implant appears in 9,787 adverse event reports: 9,734 describe injuries and 52 describe malfunctions, with 1 death. The reports mostly describe implants that fail to bond with the jawbone or later lose that bond, with some mentioning pain, infection 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
9,903
Deaths reported
1
Injuries reported
9,850
Recalls naming it
0

Summary

The FDA's MAUDE database contains 9,903 adverse event reports that list this exact device (DI 07332747161267), received between Oct 29, 2021 and Sep 30, 2026 — classified as 1 death, 9,850 injuries, 52 malfunctions.

The most frequently reported specific device problem is “Failure to Osseointegrate” (7,057 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: 167 reportsDec 2023: 168 reportsJan 2024: 190 reportsFeb 2024: 179 reportsMar 2024: 228 reportsApr 2024: 178 reportsMay 2024: 170 reportsJun 2024: 161 reportsJul 2024: 165 reportsAug 2024: 135 reportsSep 2024: 177 reportsOct 2024: 239 reportsNov 2024: 178 reportsDec 2024: 146 reportsJan 2025: 150 reportsFeb 2025: 136 reportsMar 2025: 176 reportsApr 2025: 43 reportsMay 2025: 0 reportsJun 2025: 16 reportsJul 2025: 617 reportsAug 2025: 200 reportsSep 2025: 122 reportsOct 2025: 152 reportsNov 2025: 190 reportsDec 2025: 188 reportsJan 2026: 182 reportsFeb 2026: 250 reportsMar 2026: 171 reportsApr 2026: 212 reportsMay 2026: 234 reportsJun 2026: 186 reportsJul 2026: 209 reportsAug 2026: 176 reportsSep 2026: 116 reportsOct 2026: 0 reports202420252026617
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Failure to Osseointegrate7,057
  • Loss of Osseointegration1,943
  • Osseointegration Problem532
  • Adverse Event Without Identified Device or Use Problem110
  • Fracture72
  • Patient Device Interaction Problem68
  • Migration35
  • Insufficient Device Problem Information18

Patient problems

  • Failure of Implant6,561
  • No Clinical Signs, Symptoms or Conditions2,562
  • Pain918
  • Unspecified Infection593
  • Numbness226
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available188
  • Implant Pain128
  • Inflammation94

Recent adverse event reports

The 25 most recent of 9,903 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.