MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US LPS SEGMENTAL COMPONENT 35MM; LPS AND S-ROM : KNEE ACCESSORY

Model Number	1987-07-035
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Foreign Body Reaction (1868); Pain (1994)
Date of Event	06/14/2018
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
Subject id: (b)(6).Clinical adverse event received for increased pain, abnormal radiographic evaluation indicating interval migration anterior cortex abutment of the proximal stem of the femoral component.This is noted to potentially cause a future fracture.No fracture is indicated currently.Event is serious and is considered severe.Event is definitely related to device and possibly related to procedure.Doi: (b)(6) 2011.Doe: (b)(6) 2018, (right knee).
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary = > patient product x-ray images have been provided for review (alert date: (b)(6) 2021).No device associated with this report was received for examination.Provided images are paper copies within patient medical records.Depuy synthes considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation may be re-opened as necessary.

• Brand Name: LPS SEGMENTAL COMPONENT 35MM
• Common Device Name: LPS AND S-ROM : KNEE ACCESSORY
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• Manufacturer (Section G): DEPUY ORTHOPAEDICS, INC. 1818910; 700 orthopaedic dr.; warsaw IN 46581 0988
• Manufacturer Contact: kara ditty-bovard ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 6107428552
• MDR Report Key: 12533130
• Report Number: 1818910-2021-21179
• Device Sequence Number: 12419288
• Product Code: JWH
• UDI-Device Identifier: 10603295078531
• UDI-Public: 10603295078531
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• PMA/510(K) Number: K033959
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2011
• Device Explanted Year: 2018
• 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
• Report Date (Section B): 09/01/2021

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 Model Number: 1987-07-035
• Device Catalogue Number: 198707035
• Device Lot Number: E4FCA1000
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/01/2021
• Supplement Date Received by Manufacturer: 12/07/2021
• Initial Report FDA Received Date: 09/27/2021
• Supplement Report FDA Received Date: 12/08/2021
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/29/2010
• 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: LPS DISTAL FEM COMP XSM RT; LPS FEM TO SLEEVE ADAPTER +0; LPS SEGMENTAL COMPONENT 35MM; LPS UNIV TIB HIN INS XSM 21MM; LPS XX-SM HINGE PIN; UNIVERSAL FEM SLV FUL POR 31MM; UNIVERSAL STEM 75X20MM FLUTED; UNKNOWN KNEE PATELLA; LPS DISTAL FEM COMP XSM RT; LPS FEM TO SLEEVE ADAPTER +0; LPS SEGMENTAL COMPONENT 35MM; LPS UNIV TIB HIN INS XSM 21MM; LPS XX-SM HINGE PIN; UNIVERSAL FEM SLV FUL POR 31MM; UNIVERSAL STEM 75X20MM FLUTED; UNKNOWN KNEE PATELLA
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Female
• Patient Weight: 68 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White