MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US LCS COMPLETE LOPRO POLPAT STD+; LCS COMPLETE : KNEE PATELLA

Catalog Number	129409450
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Fever (1858); Unspecified Infection (1930); Swelling (2091); Injury (2348); No Code Available (3191)
Date of Event	03/05/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.Device was used for treatment, not diagnosis.(b)(4).
Event or Problem Description
Patient presented with symptoms consistent with infection of the total knee.The patient had a fever and the operative knee was red and swollen.Surgeon drew labs and aspirated the knee.The labs were elevated consistent with infection, also the aspirate grew out bacteria.Surgeon then took the patient to surgery to remove the implants to washout and place antibiotic spacer.Implants were all well fixed.Implants were removed with very little bone loss.Antibiotic spacers were placed.Depuy cement was used.Update: depuy 2 cement ref# (b)(4) lot# 8770435 was used during the primary knee procedure on (b)(6) 2019 to cement the tibia and patella.The implants were found to be well fixed at the time of the explant procedure.Doi: (b)(6) 2019, dor: (b)(6) 2019.Left knee.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary = > no device associated with this report was received for examination.Depuy considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.If information is obtained that was not available for the initial medwatch , a follow-up medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: LCS COMPLETE LOPRO POLPAT STD+
• Common Device Name: LCS COMPLETE : KNEE PATELLA
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46582 0988
• MDR Report Key: 8451087
• Report Number: 1818910-2019-88407
• Device Sequence Number: 19589645
• Product Code: NJL
• UDI-Device Identifier: 10603295022510
• UDI-Public: 10603295022510
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 03/05/2019

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 Catalogue Number: 129409450
• Device Lot Number: 8951497
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 03/05/2019
• Supplement Date Received by Manufacturer: 03/27/2019
• Initial Report FDA Received Date: 03/26/2019
• Supplement Report FDA Received Date: 04/16/2019
• 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: Required Intervention
• Patient Age: 57 YR