PINNACLE 2218-32-652Recalls & reported problems
Depuy (Ireland) · PINNACLE TRIAL ACETABULAR LINER CON +4 NEUTRAL 32mm ID 52mm OD · Class 1
All models of PINNACLE (198)
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 10603295101116), received between Aug 15, 2017 and Feb 24, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break4
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient2
- No Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 24, 2026Break
IT WAS REPORTED THAT THE CONSTRAINED TRIAL LINER BROKE DURING SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24427291 ↗MalfunctionMay 18, 2023Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT THE THREAD ON LINER TRIAL DISCONNECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16952588 ↗MalfunctionNov 5, 2018Break; Break
LINER TRIAL BROKE AND BECAME UNUSABLE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8039447 ↗MalfunctionMay 21, 2018Break; Break
IT WAS REPORTED THAT THE CENTER SCREW RING ON TRIAL BROKE MAKING LINER TRIAL NOT USABLE. NO SURGICAL DELAY. ALL PIECES RETRIEVED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7529966 ↗MalfunctionAug 15, 2017Break; Break
IT WAS REPORTED THAT UPON POST SURGICAL EXAMINATION, BOTH CUPS WERE FOUND TO HAVE DEEP ROUGH GAUGES ON THE INSIDE AND BOTTOM SURFACE OF THE LINERS. SOME OF THE GAUGE CONTINUE TO THE EXTERIOR OF THE CUP AS WELL.
Patient problems: No Information
MAUDE report 6795691 ↗
Other TEMPLATE devices
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- 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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