Skip to content

RePlant® Precision IO Scan Adapter 6050-09PTRecalls & reported problems

Implant Direct Sybron Manufacturing LLC · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10841307123958), received between Aug 16, 2018 and Aug 16, 2018 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Inaccurate Information” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Inaccurate Information2

Patient problems

  • No Consequences Or Impact To Patient2

Recent adverse event reports

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

  • MalfunctionAug 16, 2018Inaccurate Information; Inaccurate Information

    PER INTERNAL COMPLAINT (B)(4), THE FLAT SCAN OF THE SCAN ADAPTER WAS FOUND NOT ALIGNED TO THE TRI-LOBE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7791700 ↗
  • MalfunctionAug 16, 2018Inaccurate Information; Inaccurate Information

    PER INTERNAL COMPLAINT (B)(4), THE FLAT SCAN OF THE SCAN ADAPTER WAS FOUND NOT ALIGNED TO THE TRI-LOBE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7791698 ↗

Other Accessories, Implant, Dental, Endosseous devices

All Accessories, Implant, Dental, Endosseous devices →

Sources and updates

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