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

Model Number 623-00-36F

Device Problem Unstable (1667)

Patient Problems Injury (2348); Joint Dislocation (2374); Joint Laxity (4526)

Event Date 02/13/2020

Event Type  Injury  

Manufacturer Narrative

Review of the device history records indicate that devices were manufactured and accepted into final stock with no reported discrepancies.There have been no other events for the lot referenced.If additional information is received, it will be provided in a supplemental report upon completion of the investigation.Device not returned.

Event Description

Procedure: the patient underwent right total hip arthroplasty (b)(6) 2020.Patient underwent revision right total hip for instability on (b)(6) 2020.Head, liner and stem exchanged.

Event Description

Procedure: the patient underwent right total hip arthroplasty (b)(6) 2020.Patient underwent revision right total hip for instability on (b)(6) 2020.Head, liner and stem exchanged.

Manufacturer Narrative

Reported event: an event regarding instability involving an triathlon insert was reported.The event was not confirmed by clinical review.Method & results: device evaluation and results: not performed as product was not returned.Clinician review: a review of the provided medical records by a clinical consultant stated that : one month after index tha the patient underwent revision surgery for instability.It is unclear why the stem needed to be exchanged.On the post revision xray there is a crclage wire, it is not known if this was for prohpylaxis against, or treatment for , calcar fracture.Device history review: all 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 reported lot.Conclusion: it was reported that the patient right knee was revised due to instability.A review of the provided medical records by a clinical consultant stated that : one month after index tha the patient underwent revision surgery for instability.It is unclear why the stem needed to be exchanged.On the post revision xray there is a crclage wire, it is not known if this was for prohpylaxis against, or treatment for , calcar fracture.The exact cause of the event could not be determined because insufficient information was provided.Additional information including operative reports, progress notes and return of the device are needed to fully investigate the event.If further information becomes available or the product is returned, this investigation will be re-opened.

Event Description

Procedure: the patient underwent right total hip arthroplasty (b)(6) 2020.Patient underwent revision right total hip for instability on (b)(6) 2020.Head, liner and stem exchanged.

Manufacturer Narrative

Reported event: an event regarding dislocation involving a trident liner was reported.The event was confirmed by clinical review.Method & results: device evaluation and results: not performed as product was not returned.Clinician review: a review of the provided medical records by a clinical consultant stated that : one month after index tha the patient underwent revision surgery for instability.It is unclear why the stem needed to be exchanged.On the post revision xray there is a crclage wire, it is not known if this was for "prophylaxis" against, or treatment for , calcar fracture.Further clarification from the clinician noted," dislocation of a right pressfit tha is confirmed by pre-operative x-rays.Without further confirmatory information such as an operative report and implant sheet it is not possible to be certain that the stem was revised.The stem has the same appearance and is in the same position as the pre-operative stem.However, post revision x-rays show the presence of a cerclage wire around the proximal femur.This wire would have been placed for one of two reasons.1.For prophylaxis against fracture when attempting to remove the stem or when inserting a new stem.2.A fracture did occur in the process of removal or insertion of a stem.That being stated without the documentation noted above revision of the stem can not be confirmed." device history review: all 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 reported lot.Conclusion: it was reported that the patient right hip was revised due to instability.A review of the provided medical records by a clinical consultant stated that : one month after index tha the patient underwent revision surgery for instability.It is unclear "why" the stem needed to be exchanged.On the post revision xray there is a crclage wire, it is not known if this was for "prophylaxis" against, or treatment for , calcar fracture.Dislocation of a right pressfit tha is confirmed by pre-operative x-rays.The exact cause of the event could not be determined because insufficient information was provided.Additional information including operative reports, progress notes and return of the device are needed to fully investigate the event.If further information becomes available or the product is returned, this investigation will be re-opened.

• Brand Name: TRIDENT 0 X3 INSERT 36MM ID
• Type of Device: PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
• Manufacturer (Section D): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• MDR Report Key: 10458098
• MDR Text Key: 204522097
• Report Number: 0002249697-2020-01743
• Device Sequence Number: 1
• Product Code: LPH
• UDI-Device Identifier: 07613327039535
• UDI-Public: 07613327039535
• Combination Product (y/n): N
• PMA/PMN Number: K033716
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: health professional
• Type of Report: Initial,Followup,Followup
• Report Date: 01/20/2021

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
• Device Operator: Health Professional
• Device Model Number: 623-00-36F
• Device Catalogue Number: 623-00-36F
• Device Lot Number: X803A3
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 08/03/2020
• Initial Date FDA Received: 08/27/2020
• Supplement Dates Manufacturer Received: 10/29/2020; 01/11/2021
• Supplement Dates FDA Received: 11/23/2020; 01/20/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Hospitalization; Required Intervention
• Patient Age: 48 YR
• Patient Weight: 95