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LOCATOR 02133Recalls & reported problems

Zest Anchors, LLC · LOCATOR Abutment For Narrow Internal Connection Quattro Bone Level Implant, Blue Sky Bio, 3mm Cuff · Class 2 · Implant

All models of LOCATOR (33)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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 00840481118531), received between Mar 11, 2024 and Mar 11, 2024 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 1 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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.

  • InjuryMar 11, 2024Fracture; Fracture

    CUSTOMER ORIGINAL CONTACT ZEST ON 2/13 REGARDING PART 02134 SD ABUTMENT BROKE IN THE IMPLANT DID NOT WANT REPLACEMENT AS HE WAS VERY UPSET HE JUST WANTED A REFUND. HE THEN CONTACT US TODAY 2/28 TO SAY THE OTHER ABUTMENT ALSO FRACTURED IN THE IMPLANT. IT IS UNKNOWN IF IMPLANT WAS REMOVED OR NOT DUE TO FRACTURED ABUTMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18876208 ↗

Other ABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS devices

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Sources and updates

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