MAUDE Adverse Event Report: STRYKER ORTHOPAEDICS-MAHWAH TRIATHLON P/A CR BEADED #5L; PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO

Catalog Number 5517F501

Device Problem Use of Device Problem (1670)

Patient Problem Insufficient Information (4580)

Event Date 09/27/2023

Event Type  Injury  

Event Description

A primary left tka was performed.I presented dr.With implants once bone preparations were made and appropriately sized for a ps knee.Implants were presented, read out loud and verified by size, type and expiration.Implants were implanted, patient was transferred to recovery.After the tka was finished and patient in recovery, it was brought to my attention by my usage that the incorrect femoral component was opened and implanted.Dr.Was informed.Plans were arranged for the patient to return to surgery at 4:30 the same day for a left revision tka of the femoral component and tibial insert.

Manufacturer Narrative

It was noted that the device is not available for evaluation.Should additional information become available, it will be provided in a supplemental report upon completion of the investigation.Review of the device history records indicate devices were manufactured and accepted into final stock with no relevant reported discrepancies.There have been no other similar events for the lot referenced.H3 other text : device not returned to the manufacturer.

Manufacturer Narrative

Reported event: an event regarding incorrect selection involving a triathlon femoral component was reported.The event was 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: 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 during the patient's primary surgery, a cr femoral component was implanted instead of a ps.Revision surgery took place on the same day to have the incorrect femoral component replaced.The reported event was confirmed through review of the provided implant sheet and is considered to be the result of user error as no manufacturing-related product problem was found given the information provided.No further investigation for this event is possible at this time.If additional information becomes available to indicate further evaluation is warranted, this record will be reopened.

Event Description

A primary left tka was performed.I presented dr.With implants once bone preparations were made and appropriately sized for a ps knee.Implants were presented, read out loud and verified by size, type and expiration.Implants were implanted, patient was transferred to recovery.After the tka was finished and patient in recovery, it was brought to my attention by my usage that the incorrect femoral component was opened and implanted.Dr.Was informed.Plans were arranged for the patient to return to surgery at 4:30 the same day for a left revision tka of the femoral component and tibial insert.

• Brand Name: TRIATHLON P/A CR BEADED #5L
• Type of Device: PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO
• Manufacturer (Section D): STRYKER ORTHOPAEDICS-MAHWAH; 325 corporate drive; mahwah NJ 07430
• Manufacturer (Section G): STRYKER ORTHOPAEDICS-LIMERICK; raheen business park; limerick NA ; EI NA
• Manufacturer Contact: arokiya raj ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 17972183
• MDR Text Key: 326118122
• Report Number: 0002249697-2023-01223
• Device Sequence Number: 1
• Product Code: MBH
• UDI-Device Identifier: 07613327040982
• UDI-Public: 07613327040982
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K051380
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date: 12/08/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 10/20/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 5517F501
• Device Lot Number: ATHCU
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 11/16/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 05/17/2023
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Hospitalization; Required Intervention
• Patient Age: 65 YR
• Patient Sex: Male
• Patient Weight: 101 KG