MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC COMPRESSION DEVICE/ FOR TI CANNULATED TIBIA NAILS-EX; NAIL, FIXATION, BONE

Model Number	03.010.004
Medical Device Problem Code	Device-Device Incompatibility (2919)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	01/05/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Complainant part is not expected to be returned for manufacturer review/investigation.Reporter is a synthes employee.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 on (b)(6) 2021 that the compression screw was used incorrectly in a case.Compression screw became stuck inside of connecting screw.The two screws were unable to be disconnected.The procedure was successfully completed.No surgical delayed reported.There were fragments generated and they removed easily without additional intervention.There was no reported consequence to the patient.Concomitant devices reported: cann connecting scr f/percutan instruments for nails-ex (part number 03.010.404, lot unknown, quantity.This report involves one (1) compression device/ for ti cannulated tibia nails-ex.This is report 1 of 2 for (b)(4).

• Brand Name: COMPRESSION DEVICE/ FOR TI CANNULATED TIBIA NAILS-EX
• Common Device Name: NAIL, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 11229212
• Report Number: 2939274-2021-00464
• Device Sequence Number: 3512217
• Product Code: JDS
• UDI-Device Identifier: 10886982066923
• UDI-Public: (01)10886982066923
• Combination Product (Y/N): N
• Initial Reporter State: DE
• Initial Reporter Country: US
• PMA/510(K) Number: K040762
• 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: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 01/05/2021

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: 03.010.004
• Device Catalogue Number: 03.010.004
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 01/05/2021
• Initial Report FDA Received Date: 01/26/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1