PINNACLE 1218-32-762Recalls & reported problems
Depuy Orthopaedics, Inc. · PINNACLE HIP SOLUTIONS GVF POLYETHYLENE CONSTRAINED ACETABULAR LINER +4 10 DEGREE 32mm ID 62mm OD · Class 2 · Implant
All models of PINNACLE (182)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295012047), received between May 20, 2022 and May 20, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).
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
- Device Dislodged or Dislocated1
- Fracture1
Patient problems
- Foreign Body Reaction1
- Joint Dislocation1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2022Fracture; Device Dislodged or Dislocated; Fracture; Device Dislodged or Dislocated
PATIENT UNDERWENT PRIMARY THR ON (B)(6) 2019 WHERE A CORIAL PINNACLE WAS IMPLANTED. AS PER THE NOTES, THE PATIENT DISLOCATED 2 TIMES AND WAS THEN BROUGHT BACK TO THEATRE ON (B)(6) 2019 WHERE THE PINNACLE LINER WAS EXCHANGED TO A CONSTRAINED LINER AND A LONGER FEMORAL HEAD IMPLANTED. PATIENT HAS NOW PRESENTED WITH PAIN WITH A THE X RAY SHOWING THE HIP TO BE DISLOCATED. ACCORDING TO THE PATIENT, HIS HIP HAS NEVER BEEN RIGHT AND HE HAS SUFFERED WITH PAIN SINCE THE ORIGINAL INDEX SURGERY. THE X RAY IMAGES SHOW A DISLOCATED HIP, LOCKING RING AROUND THE NECK AND THE RING THAT LOCKS THE POLY INTO THE SHELL, BROKEN AND LYING IN THE SURROUNDING SOFT TISSUE. ON OPENING THE HIP, BACKED SOFT TISSUE WAS EVIDENT, THE POLY LOCKING RING WAS LOCATED, BENT AND BROKEN AND THE POLY LINER WAS FOUND EXERTED IN THE SOFT TISSUE AND NOT IN THE SHELL. THE BLACKENED TISSUE WAS REMOVED, THE LINER REMOVED. A NEW CONSTRAINED LINER WAS IMPLANTED AND A HEAD WITHOUT A ¿SKIRT¿ IMPLANTED (THE PREVIOUS HEAD AD A SKIRT AND WOULD HAVE RESULTED IN MORE IMPINGEMENT) ONLY THE PRODUCTS REMOVED IN THIS SURGERY HAVE BEEN LISTED. DOI: (B)(6), 2019. DOR: (B)(6), 2022. RIGHT HIP.
Patient problems: Foreign Body Reaction; Joint Dislocation; Pain
MAUDE report 14461153 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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