NA 6020-29-000Recalls & reported problems
Depuy (Ireland) · ACETABULAR PUNCH · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295178538), received between Jan 14, 2020 and Jan 5, 2023 — classified as 4 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
- Contamination /Decontamination Problem1
Patient problems
- No Consequences Or Impact To Patient3
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 5, 2023Break; Break
IT WAS REPORTED WHILE GAINING ACCESS TO THE FEMORAL CANAL FOR SLEEVE INSERTION IT WAS NOTICED THAT THE INSTRUMENTS IN QUESTION WERE STARTING TO FALL APART AT THE END. ALL WOOD CHIPS FROM THE HANDLES WERE REMOVED AND THROWN AWAY. INSTRUMENTS ARE BEING RETURNED. COULD NOT FIND A LOT NUMBER ON ONE OF THE INSTRUMENTS. NO SURGICAL DELAY WAS THERE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16102218 ↗MalfunctionAug 28, 2020Contamination /Decontamination Problem; Contamination /Decontamination Problem
MORELAND SET ¿LEAKING¿ AND PRODUCING ODOR WHEN STERILIZED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10464844 ↗MalfunctionJun 4, 2020Break; Break
IT WAS REPORTED THAT THE INSTRUMENTS WERE FOUND BROKEN ON SET BY ORTHO NURSE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10118716 ↗MalfunctionJan 14, 2020Break; Break
IT WAS REPORTED THAT THE WOOD HAS CHIPPED ON HANDLE, WILL RETURN INSTRUMENT, ALL PIECES RECOVERED. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9586573 ↗
Other PUNCH, SURGICAL devices
- SIGMA LCS HIGH PERFORMANCE 9505-02-012Depuy Orthopaedics, Inc. · PUNCH, SURGICAL85 reports
- SIGMA LCS 9505-02-018Depuy Orthopaedics, Inc. · PUNCH, SURGICAL1 recall10 reports
- DJO SURGICAL 801-05-040Encore Medical, L.P. · PUNCH, SURGICAL1 recall7 reports
- SIGMA LCS 9505-02-017Depuy Orthopaedics, Inc. · PUNCH, SURGICAL1 recall1 report
- SIGMA LCS 9505-02-016Depuy Orthopaedics, Inc. · PUNCH, SURGICAL1 recall0 reports
- SIGMA LCS 9505-02-021Depuy Orthopaedics, Inc. · PUNCH, SURGICAL1 recall0 reports
- SIGMA LCS 9505-02-020Depuy Orthopaedics, Inc. · PUNCH, SURGICAL1 recall0 reports
- SIGMA HIGH PERFORMANCE 9505-02-047Depuy (Ireland) · PUNCH, SURGICAL33 reports
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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