MAUDE Adverse Event Report: STRYKER ORTHOPAEDICS-MAHWAH TRIDENT 0 DEG X3 INSERT 36MM ID E; PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

Catalog Number	623-00-36E
Medical Device Problem Code	Device Dislodged or Dislocated (2923)
Health Effect - Clinical Codes	Joint Dislocation (2374); Metal Related Pathology (4530)
Date of Event	05/17/2023
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Reported event: an event regarding dislocation involving a trident liner 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: a review of the provided medical records by a clinical consultant indicated: "confirmation of event: i can confirm that the patient had a primary left total hip arthroplasty on (b)(6) 2018 with an accolade ii femur, hi offset, and a 36 mm +5 v40 head since i was able to review the operation report.In the body of the operation, it does not mention an lfit head.In the operating room documentation, it does document a 36 mm, plus for millimeter lfit femoral head.I cannot confirm that revision was performed since i have no documentation such as office notes, operation notes or post revision x-rays.I cannot confirm any elevated levels of metal ions as no records are supplied.Root cause analysis: the root cause of this event cannot be determined with certainty.The root cause failure of a primary cementless total hip arthroplasty with an accolade stem and a cobalt chrome lfit head, approximately three years after implantation or multifactorial including surgical technique, especially in the choice of implants, preparation of the femoral head and trunnion, and insertion technique for the femoral head on the trunnion.Patient factors can contribute including lifestyle, activity level, bmi, as well as implant factors." 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 due to dislocation.Intraoperatively, "corrosion" at the stem-head interface was reported.Elevated metal ion levels was also reported.A review of the provided medical records by a clinical consultant indicated: "confirmation of event: i can confirm that the patient had a primary left total hip arthroplasty on (b)(6) 2018 with an accolade ii femur, hi offset, and a 36 mm +5 v40 head since i was able to review the operation report.In the body of the operation, it does not mention an lfit head.In the operating room documentation, it does document a 36 mm, plus for millimeter lfit femoral head.I cannot confirm that revision was performed since i have no documentation such as office notes, operation notes or post revision x-rays.I cannot confirm any elevated levels of metal ions as no records are supplied.Root cause analysis: the root cause of this event cannot be determined with certainty.The root cause failure of a primary cementless total hip arthroplasty with an accolade stem and a cobalt chrome lfit head, approximately three years after implantation or multifactorial including surgical technique, especially in the choice of implants, preparation of the femoral head and trunnion, and insertion technique for the femoral head on the trunnion.Patient factors can contribute including lifestyle, activity level, 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.
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 left hip on or about on (b)(6) 2018 and was revised on (b)(6) 2021.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 additional information received: the patient had a dislocation of the left hip on (b)(6) 2021 and revision surgery was performed on (b)(6) 2021.Intraoperatively, "corrosion" was found at the metal trunnion.It is not reported what other devices besides the metal head were revised.

• Brand Name: TRIDENT 0 DEG X3 INSERT 36MM ID E
• Common Device Name: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
• Manufacturer (Section D): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• Manufacturer (Section G): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• Manufacturer Contact: arokiya raj ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 20558654
• Report Number: 0002249697-2024-01484
• Device Sequence Number: 8980051
• Product Code: LPH
• UDI-Device Identifier: 07613327039542
• UDI-Public: 07613327039542
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: K033716
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2021
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 10/29/2024

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 Catalogue Number: 623-00-36E
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 10/11/2024
• Initial Report FDA Received Date: 10/29/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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: 80 YR
• Patient Sex: Female