MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 5.0 TI LCKNG SCR SLF-TPNG T25 SD 50-SILE; APPLIANCE, FIXATION, NAIL

Model Number	412.219S
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Pain (1994)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product complaint # (b)(4).: (b)(6).Complainant part is not expected to be returned for manufacturer review/ investigation.The investigation could not be completed, no product was received; no conclusion could be drawn at the time of filing this report.Based on the information available, it has been determined that no corrective and 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 history lot: part: 412.219s, lot: 2l28021, manufacturing site: (b)(4), supplier: n/a, release to warehouse date: 05 december 2018, expiration date: 31 october 2028.A manufacturing record evaluation was performed for the finished article lot and no non-conformances were identified.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.
Event or Problem Description
It was reported that on (b)(6) 2021, during the removal surgery, the surgeon removed the femoral neck plate, one antirotation screw, one locking screw, and one bolt.Patient was in pain and the femoral head had avn.Patient has dementia.Everything was removed successfully.The surgeon then converted this patient to a total arthroplasty.It is unknown if there was a surgical delay.It is unknown if the procedure was successfully completed.No patient consequence.This complaint involves four (4) devices.This report is for (1) 5.0 ti lckng scr slf-tpng t25 sd 50-sile.This is report 4 of 4 for complaint (b)(4).

• Brand Name: 5.0 TI LCKNG SCR SLF-TPNG T25 SD 50-SILE
• Common Device Name: APPLIANCE, FIXATION, NAIL
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• Manufacturer (Section G): WERK MEZZOVICO (CH); via cavazz 5; mezzovico 6805 ; SZ 6805
• Manufacturer Contact: kara ditty-bovard ; 1302 wright lane east; west chester, PA 19380 ; 6107195000
• MDR Report Key: 12909594
• Report Number: 2939274-2021-06879
• Device Sequence Number: 14723798
• Product Code: KTT
• UDI-Device Identifier: 10886982275462
• UDI-Public: (01)10886982275462
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K000682
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician Assistant
• Type of Report: Initial
• Report Date (Section B): 11/03/2021

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: 412.219S
• Device Catalogue Number: 412.219S
• Device Lot Number: 2L28021
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 11/03/2021
• Initial Report FDA Received Date: 12/01/2021
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 12/05/2018
• 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: ANTIROTATION SCR FEM NECK 105 LNTH - S; BOLT FOR FEMORAL NECK SYS 105 LENGTH-S; FEMORAL NECK SYSTEM PL 1 HOLE - STERILE
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 89 YR
• Patient Sex: Male