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LOCATOR 08663Recalls & reported problems

Zest Anchors, LLC · LOCATOR Abutment for 3.5mm Screw-Vent & Compatibles x 2.5mm · Class 2 · Implant

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840481101229), received between Sep 27, 2019 and Oct 18, 2019 — classified as 2 injuries.

The most frequently reported specific device problem is “Fracture” (2 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.

Most reported problems

Device problems

  • Fracture2

Patient problems

  • Failure of Implant2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryOct 18, 2019Fracture; Fracture

    DOCTOR INDICATED FRACTURE OF ABUTMENT INSIDE IMPLANT. IMPLANT WAS REMOVED.

    Patient problems: Failure of Implant

    MAUDE report 9207838 ↗
  • InjurySep 27, 2019Fracture; Fracture

    DOCTOR INDICATED FRACTURE OF ABUTMENT INSIDE PATIENT. IMPLANT WAS REMOVED.

    Patient problems: Failure of Implant

    MAUDE report 9131424 ↗

Other ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS devices

All ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.