MORELAND 2422-03-000Recalls & reported problems
Depuy Orthopaedics, Inc. · MORELAND REV INST EXTRACTION HOOK · Class 1
All models of MORELAND (22)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295123026), received between Sep 26, 2018 and Jun 16, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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
- Break3
Patient problems
- No Consequences Or Impact To Patient2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 16, 2022Break; Break
IT WAS REPORTED THAT INSTRUMENT BROKE DURING USE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14713545 ↗MalfunctionSep 28, 2018Break; Break
IT WAS REPORTED THAT THE HOOK EXTRACTOR BROKE DURING USE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7918730 ↗MalfunctionSep 26, 2018Break; Break
EXTRACTION HOOK THIS HAS FRACTURED IN TO TWO PARTS. THERE HAS BEEN NO REPORT OF DELAY IN THEATRE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7910175 ↗
Other HOOK, BONE devices
- NA 6020-13-000Depuy (Ireland) · HOOK, BONE2 reports
- V. Mueller OS4080-002Steris Corporation · HOOK, BONE1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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