DURALOC 2247-18-000Recalls & reported problems
Depuy (Ireland) · DURALOC TRIAL LINER 32mm ID 58mm OD +4 · Class 1
All models of DURALOC (23)
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 10603295108085), received between Jul 8, 2019 and Oct 2, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break2
- Component Missing1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 2, 2019Break; Component Missing; Break; Component Missing
IT WAS REPORTED THAT THE 58 +4N TRIAL LINER IS BROKEN. IT IS A DURALOC, SO VERY OLD. THREADED PART IS MISSING FROM LINER TRIAL. THE CASE WAS A 52 CUP AND THIS IS A 58 SO THERE WAS NO ISSUE IN THE CASE. THIS WAS BROUGHT TO SALES REPS ATTENTION. IT HAD NO DELAY TO THE CASE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9147296 ↗MalfunctionJul 8, 2019Break; Break
PINNACLE LINER TRIAL BROKE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8768417 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page