MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US SIG C/R POROCOAT FEM RT SZ 3; SIGMA KNEE PRIMARY : KNEE FEMORAL

Catalog Number	940023
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Discomfort (2330); Numbness (2415); Paresthesia (4421)
Date of Event	10/08/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
Subject id: (b)(6).Study no: dots: clinical adverse events received for continued pain, pinching sensation.Device and procedure(relatedness).Device related: possibly.Procedure related: remote possibility.Date of event: 8/oct/2024.Date of implant: no information provided.Date of revision: no information provided.Device location: right.Treatment/impact: surgical exploration of the femur and debridement of the fat pad.Depuy components used in procedure without date of revision: catalog id: 129433130, lot id: 9744770, component type: tibial, description: mbt cemented keel sz 3.Catalog id: 940023, lot id: j50c75, component type: femoral, description: sigma fem c/ret porocoat sz 3 rt.Catalog id: 960101, lot id: d20101506, component type: patellar, description: sigma patella oval dome 3 pegged 35mm.Catalog id: 3322020, lot id: 9524034, component type: cement, description: smart set bone cement 20g.Catalog id: 3322020, lot id: 9448053, component type: cement, description: smart set bone cement 20g.Catalog id: 196192034, lot id: 9137529, component type: insert, description: aox cvd rp tibial insert sz 3 17.5mm.The patient status post: right knee replacement/revision knee replacement.The patient initially did quite well, unfortunately, after surgery she was involved in a motor vehicle accident and then developed instability which warranted a revision.The poly insert was revised.The patient did well after surgery, but continues to have pain and discomfort around the knee.Patient also reports numbness in thigh related to meralgia paresthetica.The surgeon¿s impression is possible pinching of the fat pad with reactive bone changes proximal to the femur.The surgeon is going to explore and debride the fat pad and explore the femur.
Additional Manufacturer Narrative
Depuy orthopaedics is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy orthopaedics has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy orthopaedics or its employees that the report constitutes an admission that the device, depuy orthopaedics, 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 medwatch, a follow-up medwatch will be filed as appropriate.
Additional Manufacturer Narrative
Product complaint (b)(4).Investigation summary: no device associated with this report was received for examination.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 records evaluation (mre) was not perform.As part of our company quality system process, all devices are manufactured, inspected, and distributed to approved specifications.Additional complaint information monitoring for potential safety signals will be conducted through complaint trending as part of the post-market surveillance.If additional information is made available, the investigation will be updated as applicable.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: SIG C/R POROCOAT FEM RT SZ 3
• Common Device Name: SIGMA KNEE PRIMARY : KNEE FEMORAL
• 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: kate karberg ; 700 orthopaedic dr.; warsaw, IN 46581 ; 3035526892
• MDR Report Key: 20558629
• Report Number: 1818910-2024-22563
• Device Sequence Number: 8996586
• Product Code: MBH
• UDI-Device Identifier: 10603295223474
• UDI-Public: (01)10603295223474(17)300531(10)J50C75
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K062654
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Study,Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• 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 Catalogue Number: 940023
• Device Lot Number: J50C75
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 10/10/2024
• Supplement Date Received by Manufacturer: 10/31/2024
• Initial Report FDA Received Date: 10/29/2024
• Supplement Report FDA Received Date: 11/01/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/08/2020
• 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
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 61 YR
• Patient Sex: Female
• Patient Weight: 92 KG