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LOCATOR 02071Recalls & reported problems

Zest Anchors, LLC · LOCATOR ABUTMENT NP CONICAL CONNECTION X3.0 · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00893202000028), received between Apr 24, 2023 and Apr 24, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (1 report).

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

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • InjuryApr 24, 2023Fracture; Fracture

    LOCATOR BROKE INSIDE THE IMPLANT. CUSTOMER STATED THAT LOCATOR ABUTMENT SCREW BROKE INSIDE THE IMPLANT AND 3 YEARS AFTER PLACEMENT AND COULD NOT RETRIEVE SCREW SO IMPLANT REMOVED AND REPLACED WITH LARGER DIAMETER.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16801721 ↗

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.