DEPUY PINNACLE SECTOR W/GRIPTON ACETABULAR CUP SIZE 54 MM 1217-32-054

Adverse Event reported on 7/26/2013

Device Attributes
AttributeValue
ManufacturerDEPUY ORTHOPAEDICS, INC
Brand NameDEPUY PINNACLE SECTOR W/GRIPTON ACETABULAR CUP SIZE 54 MM
Device TypeMETAL-ON-METAL HIP IMPLANT
Product CodeKWA
Model Number1217-32-054
Catalog Number1217-32-054
Device Operator0LP
ManufacturerDEPUY ORTHOPAEDICS, INC
Brand NameMETAL INSERT
Device TypeINSERT
Product CodeLZO
Model Number
Catalog Number
Device Operator0LP
ManufacturerDEPUY ORTHOPAEDICS, INC
Brand NameAML W/FEMORAL STEM
Device TypeSTEM
Product CodeLZO
Model Number
Catalog Number
Device Operator0LP
ManufacturerDEPUY ORTHOPAEDICS, INC
Brand NameASPHERE M-SPEC FEMORAL HEAD 36 MM +5
Device TypeFEMORAL HEAD
Product CodeKXA
Model Number
Catalog Number
Device Operator0LP
DEPUY ORTHOPAEDICS, INC DEPUY PINNACLE SECTOR W/GRIPTON ACETABULAR CUP SIZE 54 MM METAL-ON-METAL HIP IMPLANT Back to Search Results
Model Number 1217-32-054
Event Date 04/28/2009
Event Type  Injury  
Event Description

On (b)(6) 2009, i underwent a left total hip arthroplasty. I received a depuy pinnacle hip system consisting of a pinnacle sector w/gripton acetabular cup size 54 mm, with the 36 mm x 54 mm metal insert, a aml small stature 155 mm length with 43 mm offset femoral stem, and an asphere m-spec femoral head 36 mm +5. Soon after this surgery, i began experiencing severe pain and discomfort. Since the implantation of the pinnacle device, i experienced severe pain and discomfort when walking, standing, and sitting. I also experienced severe pain and discomfort and inflammation in my left thigh and left hip area.

 
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