Prima 15734KRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI D76815734K0), received between May 1, 2020 and Oct 30, 2024 — classified as 8 injuries.

The most frequently reported specific device problem is “Failure to Osseointegrate” (7 reports).

5 other recalls cover devices cleared under the same FDA submission (K051614); they may or may not involve this specific model.

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 18, 2026.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjuryOct 30, 2024Failure to Osseointegrate; Failure to Osseointegrate

  FAILED TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration

  MAUDE report 20567941 ↗
• InjuryOct 18, 2024Failure to Osseointegrate; Failure to Osseointegrate

  FAILED TO OSSEOINTEGRATE

  Patient problems: Inadequate Osseointegration

  MAUDE report 20480634 ↗
• InjuryFeb 23, 2024Loss of Osseointegration; Loss of Osseointegration

  LOSS OF OSSEOINTEGRATION.

  Patient problems: Implant Pain; Inadequate Osseointegration; Unspecified Infection

  MAUDE report 18769175 ↗
• InjuryJan 17, 2024Failure to Osseointegrate; Failure to Osseointegrate

  FAILED TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration; Osteopenia/ Osteoporosis

  MAUDE report 18529522 ↗
• InjuryNov 21, 2023Failure to Osseointegrate; Failure to Osseointegrate

  FAILED TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration

  MAUDE report 18181282 ↗
• InjuryJul 6, 2023Failure to Osseointegrate; Failure to Osseointegrate

  FAILED TO OSSEOINTEGRATE.

  Patient problems: Inadequate Osseointegration

  MAUDE report 17269352 ↗
• InjuryJan 9, 2023Failure to Osseointegrate; Failure to Osseointegrate

  FAILED TO OSSEOINTEGRATE.

  Patient problems: Failure of Implant; Inadequate Osseointegration

  MAUDE report 16127326 ↗
• InjuryMay 1, 2020Failure to Osseointegrate; Failure to Osseointegrate

  FAILURE TO OSSEOINTEGRATE.

  Patient problems: Failure of Implant

  MAUDE report 10019020 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K051614. One submission often covers many models, so check the product and lot details in each record.

• Z-2162-2018 · May 1, 2018 · Terminated
  Prima Plus 4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or fully edentulous mandibles and maxillae, in support of single
• Z-0608-2018 · Jun 20, 2017 · Terminated
  Multi-Unit Abutment Angled, 17, 4mm Cuff 4.1/4.5mm TiLobe Implants, Catalog Number 45324K pRODUCT Usage: Use in partially or fully edentulous mandibles and maxillae, in support of
• Z-1818-2017 · Mar 9, 2017 · Terminated
  Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K
• Z-0299-2017 · Sep 15, 2016 · Terminated
  Keystone Dental PrimaConnex Straight Implant TC, RD Internal Connection 4.0 x 11.5mm. Product code:15613K Implants are intended for use in partially or fully edentulous mandibles a
• Z-0973-2013 · Mar 11, 2013 · Terminated
  PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed bridgework.