PINNACLE 1219-28-252Recalls & reported problems
Depuy Orthopaedics, Inc. · PINNACLE HIP SOLUTIONS MARATHON POLYETHYLENE ACETABULAR LINER LIPPED 28mm ID 52mm OD · Class 2 · Implant
All models of PINNACLE (182)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295013624), received between Oct 22, 2019 and Nov 10, 2020 — classified as 4 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Device Dislodged or Dislocated2
Patient problems
- No Code Available4
- Joint Dislocation2
- Foreign Body Reaction1
- No Consequences Or Impact To Patient1
- Pain1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryNov 10, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
InjuryAug 12, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
A. WAS THE HEAD ALSO REVISED AND IS A DEPUY PRODUCT? IF YES, PLEASE PROVIDE THE PRODUCT DETAILS. B. WHAT IS THE AFFECTED SIDE INVOLVED IN THIS EVENT? RESPONSES: THE HEAD WAS ANOTHER MANUFACTURER FOR THIS CURRENT REVISION IF I RECALL IT WAS A RIGHT HIP ALTHOUGH I CANNOT BE CERTAIN.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 10396717 ↗InjuryFeb 18, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PPF AND STICKER SHEETS RECEIVED. THERE WERE NO ALLEGATION REPORTED. DOI: (B)(6) 2006; DOR: NONE REPORTED LEFT HIP.
Patient problems: No Code Available; No Consequences Or Impact To Patient
MAUDE report 9720934 ↗InjuryOct 22, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
PPF AND MEDICAL RECORD RECEIVED. PPF ALLEGES DISLOCATION, METAL WEAR, METALLOSIS AND ELEVATED METAL IONS BEFORE FIRST REVISION. AFTER REVIEW OF MEDICAL RECORDS, THERE IS NO REVISION NOTES PROVIDED. DOI: (B)(6) 2002; DOR: (B)(6) 2003, RIGHT HIP.
Patient problems: Foreign Body Reaction; Joint Dislocation; No Code Available
MAUDE report 9218870 ↗
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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