MAUDE Adverse Event Report: SMITH & NEPHEW, INC. XR ART ISRT XLPE LAT SZ 5-6 LT 9MM -2DEG; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL

Model Number	74024025
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Injury (2348)
Date of Event	12/17/2018
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient underwent a left tkr on (b)(6) 2018.Despite physical therapy and adequate pain management, the patient was unable to maintain an acceptable post-op knee range of motion (knee stiffness).Manipulation under anesthesia was performed twice.Actions taken were: surgery, medication therapy and physical therapy.The patient gained significant rom & was able to achieve more terminal flexion.The outcome of this event is still ongoing.All available information has been disclosed.If additional information should become available, a supplemental report will be submitted accordingly.
Additional Manufacturer Narrative
H6: the device, used in treatment, was not returned for evaluation and the reported event could not be confirmed.The clinical/medical evaluation concluded that the united states reports two manipulations under anesthesia for knee stiffness and reduced range of motion.Clinical study report forms were provided for review , however they did not reveal a reason for the ¿stiffness¿.The patient gained significant rom & was able to achieve more terminal flexion.The outcome of this event is still ongoing.The impact to the patient beyond the stiffness and the two procedures was the increased range of motion.Smith and nephew has not received adequate materials (operative reports) to fully evaluate the complaint, but if additional clinically relevant materials are later received, then the case may be re-opened for further evaluation.A review of complaint history did reveal one additional complaint for the listed batch for the same failure mode.A review of the manufacturing records did not reveal a manufacturing abnormality that could have caused or contributed to the reported incident.At this time, we have no reason to suspect that the product failed to meet any product specifications at the time of manufacture.A review of the risk management file and instructions for use documents revealed this failure mode and potential harm was previously identified.Some potential probable causes could be alignment, fit/size of device used or wear.Based on this investigation, the need for corrective action is not indicated.Without the return of the actual product involved or product information, our investigation could not proceed.Should the device or additional information be received, the complaint will be reopened.No further investigation is warranted for this complaint; however, we will continue to monitor for future complaints and investigate as necessary.

• Brand Name: XR ART ISRT XLPE LAT SZ 5-6 LT 9MM -2DEG
• Common Device Name: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks rd.; memphis TN 38116
• MDR Report Key: 10356734
• Report Number: 1020279-2020-03643
• Device Sequence Number: 2399278
• Product Code: JWH
• UDI-Device Identifier: 00885556616536
• UDI-Public: 00885556616536
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: K152726
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/29/2021

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 Expiration Date: 09/17/2026
• Device Model Number: 74024025
• Device Catalogue Number: 74024025
• Device Lot Number: 16JM08911
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 07/08/2020
• Supplement Date Received by Manufacturer: 06/28/2021
• Initial Report FDA Received Date: 08/03/2020
• Supplement Report FDA Received Date: 06/29/2021
• 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