MAUDE Adverse Event Report: SYNTHES GMBH 4.5 VA-LCP CRVD COND PL/10 HOLE/230/LFT; CONDYLAR PLATE FIXATION IMPLANT

Model Number	02.124.411
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Bone Fracture(s) (1870); Pain (1994)
Type of Reportable Event	Serious Injury
Event or Problem Description
On (b)(6) 2021, the patient underwent left total knee arthroplasty with distal replacement.Hardware removal left femur due to left supracondylar/intercondylar femoral fracture nonunion, hardware failure and osteoarthritis left knee.On (b)(6) 2021 the patient underwent left distal femur open reduction and internal fixation with a synthes lateral plate and multiple cerclage cables due to left distal femur comminuted intra-articular fracture and morbid obesity.It was reported that on (b)(6) 2021, the patient had a fall.She was climbing over something like a dog gate, tripped and fell.She initially felt pain in her left knee.She was diagnosed with a left distal femur fracture.This complaint involves seven (7) devices.This report is for one (1) 4.5 va-lcp crvd cond pl/10 hole/230/lft.This is report 1 of 7 for complaint (b)(4).
Additional Manufacturer Narrative
Product complaint # (b)(4).Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If the information is unknown, not available or does not apply, the section/field of the form is left blank.Additional pro-code: hrs, hwc.Complainant part is not expected to be returned for manufacturer review/investigation.Initial reporter is lawyer.Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If the information is unknown, not available or does not apply, the section/field of the form is left blank.H6: photo investigation: the photo was returned to depuy synthes for evaluation.The depuy synthes team conducted a visual inspection of the returned device images.Visual analysis of the photo revealed that the 4.5 va-lcp crvd cond pl/10 hole/230/lft is shown broken in two pieces was implanted on the patient.Also it is shown the device broken already explanted.No other defect was found.As the device was not returned, an as-received condition could not be assessed, and a dimensional inspection and document/specification review were not completed.As part of depuy synthes quality process, all devices are manufactured, inspected, and released to approved specifications.The overall complaint was confirmed for the 4.5 va-lcp crvd cond pl/10 hole/230/lft.There is no indication that a design or manufacturing issue has caused the complaint condition and hence the root cause cannot be determined.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.: there is no device problem associated with this complaint.This complaint is adverse event only.

• Brand Name: 4.5 VA-LCP CRVD COND PL/10 HOLE/230/LFT
• Common Device Name: CONDYLAR PLATE FIXATION IMPLANT
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA 19380 ; 3035526892
• MDR Report Key: 16723761
• Report Number: 8030965-2023-04498
• Device Sequence Number: 18171855
• Product Code: JDP
• UDI-Device Identifier: 10886982042835
• UDI-Public: (01)10886982042835
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K110354
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• 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?: Yes
• Operator of Device: Health Professional
• Device Model Number: 02.124.411
• Device Catalogue Number: 02.124.411
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 03/22/2023
• Supplement Date Received by Manufacturer: 05/05/2023
• Initial Report FDA Received Date: 04/12/2023
• Supplement Report FDA Received Date: 05/08/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 2.0 FLIP ANCHOR CABLE ASSEMBLY/600-SILE; 4.5MM CORTEX SCREW SELF-TAPPING 38MM; 4.5MM CORTEX SCREW SELF-TAPPING 38MM; 5.0 VA LOCKNG SCR SLF-TPNG/SD/36; 5.0 VA LOCKNG SCR SLF-TPNG/SD/36; 5.0 VA LOCKNG SCR SLF-TPNG/SD/36; 5.0MM CANNULATED VA LOCKING SCREW/70MM; 5.0MM CANNULATED VA LOCKING SCREW/70MM; 5.0MM CANNULATED VA LOCKING SCREW/70MM; 5.0MM CANNULATED VA LOCKING SCREW/75MM; 5.0MM CANNULATED VA LOCKING SCREW/75MM; 5.0MM CANNULATED VA LOCKING SCREW/90MM; 5.0MM CANNULATED VA LOCKING SCREW/90MM; 5.0MM CANNULATED VA LOCKING SCREW/90MM
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 71 YR
• Patient Sex: Female