MAUDE Adverse Event Report: SMITH & NEPHEW, INC. JOURN ART INS BCS STD 7-8 LT13; PROSTH,KNEE,PATFEMTIB,SEMICONSTR,CEMENT,POLY/MET/POLY

Model Number	74023284
Medical Device Problem Codes	Break (1069); Fracture (1260)
Health Effect - Clinical Codes	Failure of Implant (1924); Injury (2348); Joint Laxity (4526)
Date of Event	10/08/2020
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that a patient showed instability was brought to the operating room and the post in a 7-8 left 15mm journey l bcs poly was broken or worn off.A new 15mm hi post revision poly was put in.
Additional Manufacturer Narrative
H3, h6: the device, used in treatment, was not returned for evaluation.Therefore, product analysis could not be performed at this time.So the reported event could not be confirmed.A medical investigation was conducted and confirms this case reports the patient underwent a poly insert and patella exchange, due to instability.During the revision, it was found that the post on the insert was broken/worn off.To date, the requested surgical reports and x-rays have not been provided to fully evaluate the root cause of the reported event.Therefore, patient impact beyond the revision cannot be determined.No further medical assessment is warranted at this time.Should clinically relevant documentation/information become available, the clinical/medical task may be re-evaluated.A complaint history review found related failures; this failure mode will be monitored for future complaints for any necessary corrective actions.A review of risk management files and instructions for use found that the reported failure was documented appropriately.Some potential probable causes for this event could include but not limited fit/sizing, alignment, surgical technique, joint laxity, traumatic injury and procedural/user error.At this time, we have no reason to suspect that the product failed to meet any product specifications at the time of manufacture.Based on this investigation, the need for corrective action is not indicated.Without the actual product involved and/or device information, our investigation cannot proceed.If the device or new information is received in the future, this complaint can be re-opened.No further actions are being taken at this time.We consider this investigation closed.

• Brand Name: JOURN ART INS BCS STD 7-8 LT13
• Common Device Name: PROSTH,KNEE,PATFEMTIB,SEMICONSTR,CEMENT,POLY/MET/POLY
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks rd.; memphis TN 38116
• MDR Report Key: 10789376
• Report Number: 1020279-2020-06195
• Device Sequence Number: 3016039
• Product Code: JWH
• UDI-Device Identifier: 03596010555373
• UDI-Public: 03596010555373
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• PMA/510(K) Number: K042515
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 07/15/2021

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
• Operator of Device: Health Professional
• Device Model Number: 74023284
• Device Catalogue Number: 74023284
• Device Lot Number: UNKNOWN
• Initial Date Received by Manufacturer: 10/08/2020
• Supplement Date Received by Manufacturer: 07/14/2021
• Initial Report FDA Received Date: 11/04/2020
• Supplement Report FDA Received Date: 07/15/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention