MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US LCS COMPLETE REV FEM CEM L MED; LCS REVISION : KNEE FEMORAL

Model Number	1294-29-030
Medical Device Problem Codes	Loss of or Failure to Bond (1068); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Unspecified Infection (1930); Inflammation (1932); Pain (1994); Limited Mobility Of The Implanted Joint (2671); No Code Available (3191)
Date of Event	09/10/2020
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
Patient received a lcs revision in (b)(6) some time ago (dates, surgeon and hospital unavailable) and has been experiencing increasing pain and decreased function over the last couple of months.Implants were revised in a two-stage revision for suspected infection on (b)(6) 2020.
Additional Manufacturer Narrative
Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
Event or Problem Description
Additional information received stated that there was loosening at the tibial and femoral components.
Additional Manufacturer Narrative
Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
Event or Problem Description
Additional information received confirming the infection.It was stated that there was a culture grown from the retrieved specimens that are likely to have lead to the component loosening (bug type not confirmed).
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary : no device associated with this report was received for examination.A worldwide lot specific complaint database search, or device history record (dhr) review, was not possible because the required lot number was not provided.Based on previous investigations, this complication of joint replacement is unlikely to have been the result of a device failing to meet required specifications.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.Device history lot : a worldwide lot specific complaint database search, or device history record (dhr) review, was not possible because the required lot number was not provided.

• Brand Name: LCS COMPLETE REV FEM CEM L MED
• Common Device Name: LCS REVISION : KNEE FEMORAL
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 10567504
• Report Number: 1818910-2020-20659
• Device Sequence Number: 2744116
• Product Code: NJL
• UDI-Device Identifier: 10603295025511
• UDI-Public: 10603295025511
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 09/10/2020

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?: Yes
• Operator of Device: Health Professional
• Device Model Number: 1294-29-030
• Device Catalogue Number: 129429030
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 09/10/2020
• Supplement Date Received by Manufacturer: 09/10/2020; 10/12/2020; 12/01/2020
• Initial Report FDA Received Date: 09/22/2020
• Supplement Report FDA Received Date: 09/29/2020; 10/22/2020; 12/02/2020
• 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: CTM MBT REVISION TRAY SIZE 3; LCS COMP VVC INS MED 22.5MM; LCS COMPLETE REV FEM CEM L MED; MBT TRAY SLEEVE POR M/L 37MM; UNIVERSAL FEM SLV DIS POR 31MM; UNIVERSAL STEM 75X12MM FLUTED; UNIVERSAL STEM 75X18MM FLUTED; CTM MBT REVISION TRAY SIZE 3; LCS COMP VVC INS MED 22.5M M; LCS COMPLETE REV FEM CEM L MED; MBT TRAY SLEEVE POR M/L 37 MM; UNIVERSAL FEM SLV DIS POR 31 MM; UNIVERSAL STEM 75X12 MM FLUTED; UNIVERSAL STEM 75X18 MM FLUTED
• Outcome Attributed to Adverse Event: Required Intervention