MAUDE Adverse Event Report: SYNTHES GMBH 3.2MM TROCAR; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Catalog Number	03.010.069
Medical Device Problem Code	Device-Device Incompatibility (2919)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/14/2024
Type of Reportable Event	Malfunction
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.E3: reporter is a j&j employee.H6: the subject device has been received, the investigation is in progress, no conclusion could be drawn at the time of filing 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.
Event or Problem Description
It was reported that on (b)(6) 2024, the patient underwent orif surgery with the products in question.This is a report of intraoperative interference between the drill tip and the intramedullary nail.During the surgery, after insertion of an intramedullary nail and proximal fixation, distal anterolateral screw fixation was performed.During distal posterolateral screw fixation, the drill tip interfered with the intramedullary nail.After interference, because of the possibility of force on the sleeve due to soft tissue tension, a small amount of skin incision and deployment was added.Attempted to drill again but again there was interference.The surgeon pulled out the drill and tried to drill a hole with a smaller 3.0 mm diameter k-wire, but the interference happened again.The connection between the intramedullary nail and the handle and the connection between the aiming arm and the insertion handle were checked again for looseness.There was no interference during the dry check before insertion.When checked from the side with the sleeve in place, it was clearly observed that the sleeve was displaced backward.The surgeon considered removing the aiming arm and performing the insertion by freehand, but decided against it due to the rearward insertion from the outside and the long drill tip.Eventually the interference had been resolved.The end cap was inserted and the wound was closed.There are no pieces in the patient.The surgeon confirmed by x-ray.The surgery was completed successfully with 30 minutes surgical delay.After the surgery, the drill was confirmed to have passed because the surgeon had performed a thorough soft tissue development again.Patient outcome is reported as stable.This report is for one (1) 3.2mm trocar.This is report 2 of 4 for complaint (b)(4).This complaint is related to (b)(4) which captures additional impacted devices.
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.H3, h6: the product was returned to depuy synthes for evaluation.Visual inspection of the returned device found the color marking peeling off.The reported allegation cannot be confirmed.The observed condition was identified as an end of life indicator; damage consistent with repeated use and servicing.The lifecycle requirements of the device are event related and depend on the use and inspection of the device in clinical practice.As the device can be damaged on the first or 100th use, the device must be properly inspected prior to each surgical use.Refer to the device/country specific ifu for information related to end of life, reprocessing instructions, and inspection procedures.A dimensional inspection was performed and met specifications a functional test was not performed since it was not applicable to the complaint condition.The overall complaint was not confirmed as the observed condition of the trocar ø3.2 f/03.010.064 would not contribute to the complained device issue.Based on the investigation findings, the potential cause is traced to end of life, and it has been determined that no corrective and/or preventative action is required.As part of depuy synthes quality process, all devices are manufactured, inspected, and released to approved specifications.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post-market safety surveillance activities.Device history review (dhr): part# 03.010.069 , lot # 8582518, manufacturing site: werk bettlach, supplier: na, release to warehouse date: 17 sep 2013 , expiration date: na.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.

• Brand Name: 3.2MM TROCAR
• Common Device Name: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): WERK BETTLACH (CH); muracherstrasse 3; bettlach 2544 ; SZ 2544
• Manufacturer Contact: kate karberg ; 1302 wrights lane east; west chester, PA 19380 ; 8472871282
• MDR Report Key: 19725784
• Report Number: 8030965-2024-08592
• Device Sequence Number: 8033606
• Product Code: LXH
• UDI-Device Identifier: 07611819775565
• UDI-Public: (01)07611819775565(11)130917(10)8582518
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• 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?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Catalogue Number: 03.010.069
• Device Lot Number: 8582518
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/11/2024
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 06/27/2024
• Supplement Date Received by Manufacturer: 07/30/2024
• Initial Report FDA Received Date: 07/11/2024
• Supplement Report FDA Received Date: 08/21/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/17/2013
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: AIM-ARM LAT F/MULTILOC PHN; CONNECSCR CANN F/MULTILOC HUM NAIL SYST; CONNECSCR F/MULTILOC HUM NAIL SYST F/03.; DRILL BIT Ø3.2 CALIBR L340 3FLUTE F/QUIC (QTY 2); DRILLSL 8/3.2 F/03.010.063 (QTY 2); INSERT-HANDLE F/MULTILOC HUM NAIL SYST; MULTILOC PHN Ø9.5 LE CANN L160 TAN; PROTECT SLEEVE 12/8 L188 (QTY 2); TROCAR Ø3.2 F/03.010.064; UNK - GUIDE/COMPRESSION/K-WIRES; UNK - SCREWS: TRAUMA
• Patient Sex: Unknown