MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 1.6MM THREADED GUIDE WIRE 150MM; WIRE, SURGICAL

Model Number	292.72
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Patient Involvement (2645)
Date of Event	11/12/2018
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional product code: jdw.Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.510k pre-amen.Without a lot number the device history records review could not be completed.The investigation could not be completed; no conclusion could be drawn, as no product was received.The investigation could not be completed; no conclusion could be drawn, as no product was received.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) 2018, during a left elbow procedure the threaded guide wire broke off and the partially threaded screw sheared off.The head of the unknown fully threaded screw broke off.Pieces was left in the patient.There was a thirty to forty minutes delayed in the procedure and was completed successfully.Patient status was stable.There was no plan for another surgery to get the pieces out of the patient.This report is one (1) guide wire.This complaint involves three (3) devices.This report is 1 of 3 for pc-(b)(4).
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.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.H6: visual inspection: the x-ray of the 1.6 mm threaded guide wire 150 mm (part # 292.72, lot unknown) was received at us cq.Per the medical safety officer, the guide wire broke, and the device is embedded in the patient.The remainder of the guide wire was not returned to us cq.This is consistent with the reported complaint condition, thus confirming the complaint.Dimensional inspection: dimensional analysis was not performed as the relevant part was not returned.Document/specification review: the relevant drawing(s) was reviewed; a dhr review and material review could not be performed as the lot number is unknown.Conclusion: the complaint condition is confirmed as the x-ray of the 1.6 mm threaded guide wire 150 mm (part # 292.72, lot unknown) was received showing the guide wire broken off and the rest of the device embedded in the patient.There is no indication that a design or manufacturing issue contributed to the complaint.While no definitive root cause could be determined it is possible that the device encountered unintended forces.No new malfunctions were observed during the course of this investigation.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post market safety surveillance activities.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.D10: complainant part is not expected to be returned for manufacturer review/investigation.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.

• Brand Name: 1.6MM THREADED GUIDE WIRE 150MM
• Common Device Name: WIRE, SURGICAL
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 8117466
• Report Number: 2939274-2018-55172
• Device Sequence Number: 1487174
• Product Code: LRN
• UDI-Device Identifier: 10886982180889
• UDI-Public: (01)10886982180889
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 11/12/2018

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: 292.72
• Device Catalogue Number: 292.72
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 11/12/2018
• Supplement Date Received by Manufacturer: 12/04/2018; 01/08/2019
• Initial Report FDA Received Date: 11/29/2018
• Supplement Report FDA Received Date: 12/21/2018; 01/08/2019
• Patient Sequence Number: 1
• Patient Age: 36 YR
• Patient Weight: 97