PINNACLE 2218-32-754Recalls & reported problems
Depuy (Ireland) · PINNACLE TRIAL ACETABULAR LINER CON +4 10 DEG 32mm ID 54mm OD · Class 1
All models of PINNACLE (198)
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 10603295101147), received between Oct 12, 2017 and Mar 27, 2024 — classified as 3 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.
Reports received per month
Most reported problems
Device problems
- Break2
- No Apparent Adverse Event1
Patient problems
- Insufficient Information1
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 27, 2024No Apparent Adverse Event; No Apparent Adverse Event
THE INSTRUMENTS WERE REPORTED FOR AN UNKNOWN REASON. VISUAL INSPECTION OF THE RETURNED SAMPLE REVEALED THAT THE PINTRL LNR CON10DEG+4 32ID54OD WAS OBSERVED BROKEN AROUND THE SNAP RING.
Patient problems: Insufficient Information
MAUDE report 18985560 ↗MalfunctionJun 17, 2020Break; Break
IT WAS REPORTED THAT THE PINNACLE LINER CONSTRAINED 10 DEG+4. ALL PARTS WERE RETRIEVED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10160950 ↗MalfunctionOct 12, 2017Break; Break
IT WAS REPORTED THAT UPON POST SURGICAL EVALUATION, TRIAL LINER WAS FOUND TO HAVE MANY DAMAGING GOUGES TO THE BOTTOM, EXTERIOR AND BOTTOM OF THE INSTRUMENT.
Patient problems: No Information
MAUDE report 6944517 ↗
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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