MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC SPIRAL BLADE AIMING ARM FOR TI CANNULATED HUMERAL NAILS-EX; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Model Number	03.010.055
Medical Device Problem Code	Device-Device Incompatibility (2919)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/12/2022
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Complainant part is not expected to be returned for manufacturer review/investigation.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.
Event or Problem Description
It was reported that a revision surgery occurred on (b)(6) 2022.The revision was of humeral ex nail as original surgery showed that proximal locking screw missed the nail.A proximal spiral blade was placed in to stabilize.No hardware was removed.The original implants were originally implanted approximately 6 months prior.Exact implant date is unknown.It is unknown if there was a surgical delay.Procedure and patient status is unknown.This is report 3 of 3 for (b)(4).This report is for a spiral blade aiming arm.

• Brand Name: SPIRAL BLADE AIMING ARM FOR TI CANNULATED HUMERAL NAILS-EX
• Common Device Name: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• Manufacturer (Section G): WERK HÄGENDORF (CH); im bifang 6; haegendorf 4614 ; SZ 4614
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA 19380 ; 3035526892
• MDR Report Key: 14341715
• Report Number: 2939274-2022-01685
• Device Sequence Number: 15016644
• Product Code: LXH
• UDI-Device Identifier: 10886982067272
• UDI-Public: (01)10886982067272
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 03.010.055
• Device Catalogue Number: 03.010.055
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/12/2022
• Initial Report FDA Received Date: 05/09/2022
• Is the Device Labeled for Single Use? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CANN CONNECTING SCR F/ TI CANN HUM NL; INSRT H&LE FOR TI CANN HUMERAL NAILS-EX
• Patient Age: 80 YR
• Patient Sex: Male