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CHARLOTTE 44180025Recalls & reported problems

Wright Medical Technology, Inc. · 7.0 MUC Handle Quick Connect · Class 1

All models of CHARLOTTE (5)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840420191779), received between Feb 2, 2022 and Feb 2, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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 18, 2026.

Most reported problems

Device problems

  • Break1
  • 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.

  • MalfunctionFeb 2, 2022Break; Fracture; Break; Fracture

    IT WAS REPORTED THAT THE SURGEON WAS PUTTING IN THE NAIL SCREWS WITH THE RATCHETING HANDLE AND SAID THE HANDLE WAS BROKEN. THIS WAS AFTER PUTTING IN SEVERAL SCREWS. USED A SYNTHES T- HANDLE AND HAD ABOUT A 10 MIN DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13424217 ↗

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Sources and updates

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