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LOCATOR R-Tx 31806-05Recalls & reported problems

Zest Anchors, LLC · LOCATOR R-Tx Abutment for 4.2mm Platform Internal Hex Connection SICinvent Implant, SIC, 5mm Cuff · Class 2 · Implant

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 00840481121449), received between Aug 28, 2019 and Aug 28, 2019 — 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.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page