LOCATOR 01699Recalls & reported problems
Zest Anchors, LLC · LOCATOR Abutment for 3.4 Tall, Anthogyr · Class 2 · Implant
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00840481104299), received between Oct 8, 2019 and May 4, 2022 — classified as 4 injuries.
The most frequently reported specific device problem is “Fracture” (4 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
- Fracture4
Patient problems
- Failure of Implant3
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMay 4, 2022Fracture; Fracture
BREAKAGE OF THE ABUTMENT IN THE IMPLANT. NO INFORMATION ABOUT THE REMOVAL OF THE TIP. FRACTURE.
Patient problems: Insufficient Information
MAUDE report 14280991 ↗InjuryNov 9, 2021Fracture; Fracture
BROKEN ABUTMENT INSIDE THE IMPLANT. BREAKAGE OF THE ABUTMENT IN THE IMPLANT. NO INFORMATION ABOUT THE REMOVAL OF THE TIP.
Patient problems: Failure of Implant
MAUDE report 12782981 ↗InjuryNov 9, 2021Fracture; Fracture
BROKEN ABUTMENT INSIDE THE IMPLANT. BREAKAGE OF THE ABUTMENT IN THE IMPLANT. NO INFORMATION ABOUT THE REMOVAL OF THE TIP.
Patient problems: Failure of Implant
MAUDE report 12782980 ↗InjuryOct 8, 2019Fracture; Fracture
LOCATOR BREAK INSIDE IMPLANT - FAILURE OF THE BROKEN SCREW REMOVAL KIT - IMPLANT INSTALLATION PARALLEL.
Patient problems: Failure of Implant
MAUDE report 9166735 ↗
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- Esthetic Abutment 36669Nobel Biocare AB · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall2 reports
- CERTAIN® BELLATEK® IEDAT5ZimVie US Corp LLC · ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS1 recall1 report
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.