DURALOC 2237-50-000Recalls & reported problems
Depuy (Ireland) · DURALOC SCREW-IN TRIAL LINER 28mm ID 50mm OD 10 DEGREE · Class 1
All models of DURALOC (23)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295106746), received between Aug 17, 2017 and Oct 1, 2018 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Component Missing” (4 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
- Component Missing4
- Break2
Patient problems
- No Consequences Or Impact To Patient4
- No Information4
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 1, 2018Break; Component Missing; Break; Component Missing
IT WAS REPORTED THAT THE METAL PIECE MISSING FROM CENTER OF LINER TRIAL.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7921769 ↗MalfunctionOct 11, 2017Component Missing; Component Missing
COMPLAINT DESCRIPTION: IT WAS REPORTED THAT UPON INSPECTING CASE POST SURGERY IT WAS DISCOVERED 3 TRIAL LINERS WERE SCRATCHED AND DENTED BADLY. UPON REVIEW OF THE RECEIVED INSTRUMENTS IT WAS NOTED THAT THERE WERE GOUGES.
Patient problems: No Consequences Or Impact To Patient; No Information
MAUDE report 6941838 ↗MalfunctionOct 11, 2017Component Missing; Component Missing
COMPLAINT DESCRIPTION: IT WAS REPORTED THAT UPON INSPECTING CASE POST SURGERY IT WAS DISCOVERED 3 TRIAL LINERS WERE SCRATCHED AND DENTED BADLY. UPON REVIEW OF THE RECEIVED INSTRUMENTS IT WAS NOTED THAT THERE WERE GOUGES.
Patient problems: No Consequences Or Impact To Patient; No Information
MAUDE report 6941828 ↗MalfunctionOct 11, 2017Component Missing; Component Missing
COMPLAINT DESCRIPTION: IT WAS REPORTED THAT UPON INSPECTING CASE POST SURGERY IT WAS DISCOVERED 3 TRIAL LINERS WERE SCRATCHED AND DENTED BADLY. UPON REVIEW OF THE RECEIVED INSTRUMENTS IT WAS NOTED THAT THERE WERE GOUGES.
Patient problems: No Consequences Or Impact To Patient; No Information
MAUDE report 6941820 ↗MalfunctionAug 17, 2017Break; Break
IT WAS REPORTED THAT THE SCREWS ARE BROKEN OUT OF TRIAL. SURGEONS ARE COMPLAINING.
Patient problems: No Information
MAUDE report 6801520 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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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