MAUDE Adverse Event Report: DEPUY IRELAND - 9616671 ATTUNE PS RP INSRT SZ 8 10MM; ATTUNE IMPLANT : KNEE TIBIAL INSERT

Model Number	1516-50-810
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Adhesion(s) (1695); Osteolysis (2377)
Date of Event	05/12/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product complaint #: (b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
It was reported thru email by the patient as "to whom it may concern.Can you please tell me if there is any compensation for victims of failed knee replacements outside of taking legal action? i am looking for help covering my expenses for a revision surgery i had to have.Thank you." on (b)(6) 2014, the patient had a left total knee arthroplasty to address end-stage valgus arthritis.Depuy components, including depuy patella and depuy cement x2 were used during this procedure.On (b)(6) 2021, the patient had a tibial revision, left total knee to address aseptic loosening.The tibial tray was noted to have debonded from the cement and was in varus collapse.During the procedure the surgeon reported removal of fibrotic and osteolytic membrane from the bone.The insert was revised, while the femoral component and patella remained in-situ.Doi: (b)(6) 2014, dor: (b)(6) 2021, left knee.
Additional Manufacturer Narrative
Product complaint #(b)(4).Investigation summary: no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot: the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.

• Brand Name: ATTUNE PS RP INSRT SZ 8 10MM
• Common Device Name: ATTUNE IMPLANT : KNEE TIBIAL INSERT
• Manufacturer (Section D): DEPUY IRELAND - 9616671; loughbeg ringaskiddy co.; cork ; EI
• MDR Report Key: 12369927
• Report Number: 1818910-2021-18695
• Device Sequence Number: 14456708
• Product Code: NJL
• UDI-Device Identifier: 10603295052883
• UDI-Public: 10603295052883
• Combination Product (Y/N): N
• Initial Reporter State: AR
• Initial Reporter Country: US
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2014
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 08/03/2021

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: 08/31/2017
• Device Model Number: 1516-50-810
• Device Catalogue Number: 151650810
• Device Lot Number: 3498641
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 08/03/2021
• Supplement Date Received by Manufacturer: 09/16/2021
• Initial Report FDA Received Date: 08/26/2021
• Supplement Report FDA Received Date: 09/20/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: ATTUNE MEDIAL DOME PAT 41MM.; ATTUNE PS FEM LT SZ 8 CEM.; ATTUNE PS RP INSRT SZ 8 10MM.; ATTUNE RP TIB BASE SZ 7 CEM.; SMARTSET GMV 40G US EO.; SMARTSET GMV 40G US EO.; ATTUNE MEDIAL DOME PAT 41MM; ATTUNE PS FEM LT SZ 8 CEM; ATTUNE PS RP INSRT SZ 8 10MM; ATTUNE RP TIB BASE SZ 7 CEM; SMARTSET GMV 40G US EO; SMARTSET GMV 40G US EO
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 62 YR