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MORELAND 2422-01-000Recalls & reported problems

Depuy Orthopaedics, Inc. · MORELAND REV INST STD FEMORAL EXTRACTOR STD · Class 1

All models of MORELAND (22)

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 10603295123002), received between Jul 12, 2023 and Jul 21, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Naturally Worn” (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

  • Naturally Worn2
  • Device-Device Incompatibility1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

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

  • MalfunctionJul 21, 2023Naturally Worn; Naturally Worn

    IT WAS REPORTED THAT A CORAIL EXTRACTOR HAS DAMAGE ON THE THREADS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17369939 ↗
  • MalfunctionJul 12, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn

    ADDITIONAL INFORMATION RECEIVED. A. WAS THERE ANY SURGICAL DELAY RELATED TO THE EVENT? NO. B. PLEASE CONFIRM, WHEN THE EVENT OCCURRED? POST OP.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17304751 ↗

Other EXTRACTOR devices

All EXTRACTOR devices →

Sources and updates

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