PINNACLE 1218-32-656Recalls & reported problems
Depuy Orthopaedics, Inc. · PINNACLE HIP SOLUTIONS GVF POLYETHYLENE CONSTRAINED ACETABULAR LINER +4 NEUTRAL 32mm ID 56mm OD · Class 2 · Implant
All models of PINNACLE (182)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295011880), received between Sep 30, 2019 and Nov 20, 2023 — classified as 5 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated4
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Joint Dislocation4
- No Code Available2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryNov 20, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT WAS REVISED DUE TO DISLOCATED HIP. IT WAS UNKNOWN IF THERE WAS ANY SURGICAL DELAY. DOI: (B)(6) 2023. DOR: (B)(6) 2023. AFFECTED SIDE: LEFT HIP.
Patient problems: Joint Dislocation
MAUDE report 18168718 ↗InjuryFeb 25, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
REVISION OF THR - RIGHT SIDE. PATIENT HAS BILATERAL HIP REPLACEMENTS AND A HISTORY OF CHRONIC REPEATED DISLOCATION. DOI: (B)(6) 2021. DOR: (B)(6) 2021. RIGHT HIP. THIS PC WAS LINK TO: (B)(4) - (B)(6) 2017 RIGHT SIDE. (B)(4) - (B)(6) 2022 LEFT SIDE. (B)(4) - (B)(6) 2022 RIGHT SIDE. (B)(4) - (B)(6) 2022 RIGHT SIDE. (B)(4) - (B)(6) 2021 LEFT SIDE.
Patient problems: Joint Dislocation
MAUDE report 13599526 ↗InjuryMay 26, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION DUE TO INFECTION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11886826 ↗InjurySep 9, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
PATIENT HAD DISLOCATED TOTAL HIP JOINT REPLACEMENT.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 10511122 ↗InjurySep 30, 2019Device Dislodged or Dislocated; Device Dislodged or Dislocated
PPF AND STICKER SHEETS RECEIVED. PPF ALLEGES DISLOCATION WITH OPEN REDUCTION AFTER FIRST REVISION. DOI: (B)(6) 2010; DOR: (B)(6) 2013 (LEFT HIP); (B)(4) 1ST REVISION.
Patient problems: Joint Dislocation; No Code Available
MAUDE report 9136372 ↗
Other Prosthesis, hip, constrained, cemented or uncemented, metal/polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall11 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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