MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US PFCSIGMA 3POST RDDOME PAT 41MM; SIGMA KNEE PRIMARY : KNEE PATELLA

Catalog Number	960113
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Cellulitis (1768); Erythema (1840); Pain (1994)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product complaint #(b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803 (and/or part 4, as applicable).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 j&j medtech, or its employees that the report constitutes an admission that the product, j&j medtech, 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
It was reported that the patient presented with increased pain, redness, and mild erythema.Iv antibiotics was started for treatment of possible cellulitis.Affected side: right knee.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary = > a manufacturing record evaluation were performed for the finished device dhr 960113/(b)(4).It was manufactured on 25-aug-2012.Total (b)(4) parts were manufactured per specification and all raw materials met specification.After searching "(b)(4)" in etq, no record is displayed.After searching "pfc sigma round dome patella" in etq, no record is displayed.After searching "(b)(4)" in sap by (b)(4), no internal lock record is displayed.Hereby drawing a conclusion that no non-conformances were identified for this batch of products.Please provide: 1.Quantity of manufactured-(b)(4).2.Date of manufacturing-25-aug-2012 3.Expiry date-31-aug-2017 4.Any anomalies or deviations identified in dhr: none 5.Ifu reference: msa090200786 device history lot = > pfcsigma 3post rddome pat 41mm product code:-960113 lot no:-d12082207 quantity of manufactured- (b)(4).Date of manufacturing-25-aug-2012 expiry date-31-aug-2017 any anomalies or deviations identified in dhr: none ifu reference:msa090200786.Device history review = > a manufacturing record evaluation was performed for the finished device [lot/serial/batch] number, and no non-conformances / manufacturing irregularities were identified.Added: d10 concomitant corrected: h4.

• Brand Name: PFCSIGMA 3POST RDDOME PAT 41MM
• Common Device Name: SIGMA KNEE PRIMARY : KNEE PATELLA
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• Manufacturer (Section G): JTE WARSAW MFG SITE; 700 orthopaedic drive; warsaw IN 46582
• Manufacturer Contact: elba bello ; 700 orthopaedic dr.; warsaw, IN 46581 ; 9083863534
• MDR Report Key: 21996047
• Report Number: 1818910-2025-07528
• Device Sequence Number: 4312036
• Product Code: JWH
• UDI-Device Identifier: 10603295232698
• UDI-Public: (01)10603295232698(17)170831(10)D12082207
• Combination Product (Y/N): N
• Initial Reporter State: VA
• Initial Reporter Country: US
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2012
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup

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 Catalogue Number: 960113
• Device Lot Number: D12082207
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/16/2025
• Supplement Date Received by Manufacturer: 05/20/2025
• Initial Report FDA Received Date: 05/09/2025
• Supplement Report FDA Received Date: 05/21/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/25/2012
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: DEPUY1 GENTAMICIN CEMENT 40G; MBT CEM KEEL TIB TRAY SZ3; PFC SIGMARP STB TB IN 4 10.0; SIGMA PS CEM FEM SZ4N R
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Female