MAUDE Adverse Event Report: STRYKER ORTHOPAEDICS-MAHWAH 32MM -4 V40 TAPER VIT HEAD; JDI PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED

Catalog Number	6260-5-032
Medical Device Problem Codes	Corroded (1131); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Foreign Body Reaction (1868); Necrosis (1971); Pain (1994); Metal Related Pathology (4530)
Date of Event	06/23/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Reported event: an event regarding abnormal ion level involving an unknown metal head was reported.The event was not confirmed.Method & results: -product evaluation and results: material analysis, visual, functional and dimensional inspections could not be performed as the device was not returned.-clinician review: no medical records were received for review with a clinical consultant.-product history review: could not be performed as the device lot details were not provided.-complaint history review: could not be performed as the device lot details were not provided.Conclusions: it was reported that the patient was revised due to elevated metal ion levels.The exact cause of the event could not be determined because insufficient information was provided.Further information such as return of the device, pathology reports, pre- and post-operative x-rays and the revision operative report as well as patient history and follow-up notes are needed to complete the investigation for determining root cause.No further investigation for this event is possible at this time.If devices and/or additional information become available to indicate further evaluation is warranted, this record will be reopened.
Event or Problem Description
It was reported through the filing of a lawsuit that allegedly the patient was implanted with an lfit anatomic cocr v40 femoral head on her right hip on or about (b)(6) , 2011 and was revised on (b)(6) 2022.It is further alleged that she suffered injuries as a result of implantation and explantation of the device at issue, device recall and excessive levels of chromium and cobalt in her blood.
Event or Problem Description
It was reported, through the filing of a lawsuit.That allegedly, the patient was implanted with an lfit anatomic cocr v40 femoral head on her right hip on or about (b)(6) 2011.And was revised on (b)(6) 2022.It is further, alleged, that she suffered injuries as a result of implantation and explantation of the device at issue.Device recall and excessive levels of chromium and cobalt in her blood.Update: per medical records received.Patient also exhibited altr.Corrosion was observed, at the stem-head interface intraoperatively.The trunnion was wiped clean and the stem was left implanted, as it was well-fixed.The shell was also revised, as the surgeon felt the patient "would benefit from revision to a larger cup.Which is more anteverted less vertical".
Additional Manufacturer Narrative
Reported event: an event regarding altr and corrosion involving a metal head was reported.The event was confirmed, via clinician review of the provided medical records.Method & results: product evaluation and results: material analysis, visual, functional and dimensional inspections could not be performed, as the device was not returned.Clinician review: a review of the provided medical records, by a clinical consultant indicated: "this product inquiry concerns a female patient, who underwent a primary total hip arthroplasty in 2011, with an accolade stem and a cocr femoral head.Patient developed symptoms and signs consistent with trunnion/head corrosion and altr.Approximately (b)(6) years after the initial procedure, the patient required revision.I can confirm, that the patient had the primary procedure and the revision procedure, since i was able to review the operation reports for each.The root cause of this event cannot be determined, with certainty.The root causes of trunnion/head corrosion and altr are multifactorial including surgical technique.Especially, the preparation or lack thereof, the femoral head and trunnion before insertion.No particular preparation was performed in this case.Also contributing could be the patient's activity level and bmi, as well as implant factors".Product history review: review of the device history records, indicate devices were manufactured and accepted into final stock with no relevant reported discrepancies.Complaint history review: there have been no other similar events for the lot referenced.Conclusions: it was reported, that the patient was revised, due to elevated cobalt and chromium levels, altr and corrosion.The shell was also, revised to improve positioning and increase to a greater size for more optimal liner and head options.A review of the provided medical records, by a clinical consultant indicated: "this product inquiry concerns a female patient, who underwent a primary total hip arthroplasty in 2011 with an accolade stem and a cocr femoral head.Patient developed symptoms and signs consistent with trunnion/head corrosion and altr.Approximately, (b)(6) years after the initial procedure, the patient required revision.I can confirm, that the patient had the primary procedure and the revision procedure, since i was able to review the operation reports for each.The root cause of this event cannot be determined, with certainty.The root causes of trunnion/head corrosion and altr are multifactorial including surgical technique.Especially, the preparation or lack thereof, the femoral head and trunnion before insertion.No particular preparation was performed in this case.Also contributing, could be the patient's activity level and bmi, as well as implant factors".No further, investigation for this event is possible at this time.If devices and/or additional information, become available to indicate further evaluation is warranted, this record will be reopened.

• Brand Name: 32MM -4 V40 TAPER VIT HEAD
• Common Device Name: JDI PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED
• Manufacturer (Section D): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• Manufacturer (Section G): STRYKER ORTHOPAEDICS-CORK; ida industrial estate; carrigtwohill NJ NA ; EI NA
• Manufacturer Contact: anna ryan ; raheen business park; limerick NA ; EI NA ; 61498200
• MDR Report Key: 16812423
• Report Number: 0002249697-2023-00416
• Device Sequence Number: 12188615
• Product Code: JDI
• UDI-Device Identifier: 07613327012842
• UDI-Public: 07613327012842
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: K173499
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2011
• Device Explanted Year: 2022
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 01/14/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 03/31/2016
• Device Catalogue Number: 6260-5-032
• Device Lot Number: 36064703
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 03/30/2023
• Supplement Date Received by Manufacturer: 12/20/2023
• Initial Report FDA Received Date: 04/25/2023
• Supplement Report FDA Received Date: 01/14/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 03/01/2011
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 81 YR
• Patient Sex: Female